Medical devices
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2,589 medical device recalls FDA’s Enforcement Report published in 2026, the newest year, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 6, 2026.
2,589of 2,589 medical device recallsshown with your filters
The list
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530A Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS CDS982269K CDS982269L CDS982269M… Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
- Medical device recall SYRINGE LUER LOK 10CC-200/BOX BD A single lot of expired syringes were distributed due to a distribution system control failure. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement Report3 statesnamed in where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereCalifornia, Florida and Pennsylvania
- Medical device recall Reprocessed Electrophysiology Catheters and Ultrasound Catheters Expansion of RES 98277. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide, and Texas named
- Medical device recall Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Housing Components with the below product descriptions and… The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement Report3 statesnamed in where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereMinnesota, North Carolina and Texas
- Medical device recall Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and… The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement Report3 statesnamed in where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereMinnesota, North Carolina and Texas
- Medical device recall Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973,… Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 6 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Colorado, Florida, Indiana, Pennsylvania and Utah named
- Medical device recall A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, surgical convenience kit Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide, and California, Georgia, Pennsylvania and Washington named
- Medical device recall A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide, and California, Georgia, Pennsylvania and Washington named
- Medical device recall A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical convenience kit Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide, and California, Georgia, Pennsylvania and Washington named
- Medical device recall A M S, ALIGNED MEDICAL SOLUTIONS, Dr Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide, and California, Georgia, Pennsylvania and Washington named
- Medical device recall GC Agar Base Reduced or no recovery of some strains of Neisseria gonorrhoeae. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medtronic Harmony Delivery Catheter System Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall IntelliCuff, Portable automatic cuff pressure controller Due to reported complaints, the cuff device may alarm with a “Cuff System Leakage” error. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Colorado, Florida, Georgia, Hawaii, Illinois, Kentucky, Massachusetts, Michigan, North Dakota, Nebraska, New York, Ohio, Pennsylvania, Puerto Rico, South Dakota, Texas, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall CRE Pro Wireguided 6-8mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Pro Wireguided 8-10mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Pro Wireguided 10-12mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Pro Wireguided 12-15mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Pro Wireguided 15-18mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Pro Wireguided 18-20mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Wireguided 6-8mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Wireguided 8-10mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Wireguided 10-12mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Wireguided 12-15mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Wireguided 15-18mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CRE Wireguided 18-20mm 240cm Potential sterile breach of the pouches in which devices are packaged. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Adapter for Head Positioning The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Maryland, Minnesota and Pennsylvania named
- Medical device recall Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb… Due to out-of-specification, or potential out-of-specification, levels of endotoxins Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall ARTIS icono biplane Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall ARTIS icono ceiling Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall ARTIS icono floor Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement Report18 statesnamed in where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereArizona, California, Colorado, Florida, Hawaii, Illinois, Indiana, Maryland, Michigan, Minnesota, Missouri, North Carolina, New Jersey, New York, Oregon, Pennsylvania, Texas and Virginia
- Medical device recall RayCare 2024A SP1 Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall RayCare 2024A SP4 Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall ARTIS icono ceiling Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 10 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Georgia, Iowa, Indiana, Louisiana, Missouri, North Carolina, New York, Pennsylvania and South Carolina named
- Medical device recall Zeiss Intrabeam Spherical Applicator 1.5 cm Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Florida and Puerto Rico named
- Medical device recall Covidien Shiley Disposable Decannulation Plug Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, US Virgin Islands, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites Due to engineering sample labeled “Not for Human Use” being inadvertently shipped it the U.S. Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportIllinoisthe one state its words name PublishedJul 8, 2026ClassClass IIStatusOngoingWhereIllinois
- Medical device recall OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 The… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylets provide… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC SV Catheter 3 Fr… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code:… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729 PowerMidline Catheter 4… Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by… Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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