Medical devices, 2016
Shortlist up to four to read them side by side.
3,246 medical device recalls FDA’s Enforcement Report published in 2016, 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 7, 2026.
3,246of 3,246 medical device recallsshown with your filters
The list
- Medical device recall Integra External Fixation System Universal Wire Fixation Bolt - 17.5 mm Catalogue #12224218 Through the investigation of reported complaints Integra verified that there have been instances where the Universal Wire Fixation Bolts the Slotted Post broke… Class IIFDA’s classAug 17, 2016in FDA’s Enforcement Report6 statesnamed in where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereColorado, District of Columbia, Florida, Indiana, Oklahoma and Virginia
- Medical device recall Integra External Fixation System Slotted Post - Small Catalogue #12224228 Through the investigation of reported complaints Integra verified that there have been instances where the Universal Wire Fixation Bolts the Slotted Post broke… Class IIFDA’s classAug 17, 2016in FDA’s Enforcement Report6 statesnamed in where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereColorado, District of Columbia, Florida, Indiana, Oklahoma and Virginia
- Medical device recall EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80, iM50, M50, iM70, iM60, iM8, iM8A, iM8B Patient… Incorrect CO2 readings with some patient monitors. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and California, Florida and Kentucky named
- Medical device recall Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess 12mm, Synthes 2.4mm Titanium Locking… It was reported that the specified lots of the 2.4mm Titanium Locking Screw Self-Tapping with Stardrive Recess 12mm can break between the head and the shaft. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement Report17 statesnamed in where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereArkansas, California, Colorado, Delaware, Florida, Georgia, Iowa, Illinois, Kentucky, Louisiana, Minnesota, New Jersey, Oklahoma, Pennsylvania, South Dakota, Tennessee and Washington
- Medical device recall Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with Secondary Lock, Non-Sterile, Used to… It was reported that the secondary locking mechanism, and its corresponding components, disassociated from the Specialty Triathlon Tibial Alignment Handle with… Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and Florida, Indiana, Louisiana, North Carolina, Pennsylvania, Tennessee and Utah named
- Medical device recall Coolife Sinergy Radiofrequency Kit, SIK-17-75-4 Mismatch between the length of the RF electrode (probe) and the cannula (introducer), Class IIFDA’s classAug 17, 2016in FDA’s Enforcement Report8 statesnamed in where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereConnecticut, Illinois, Massachusetts, Michigan, North Carolina, New Hampshire, Nevada and Texas
- Medical device recall Hitachi Scenaria Computed Tomography System Hitachi Medical Systems America, Twinsburg, OH 44087 The firm discovered that the centrifugal force applied to the power supply may cause it to fail over time. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement Report15 statesnamed in where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereCalifornia, Florida, Georgia, Iowa, Illinois, Indiana, Maryland, North Carolina, New York, Ohio, Pennsylvania, South Dakota, Tennessee, Texas and Wyoming
- Medical device recall AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis… The possibility exists for contaminants, in the form of biomass, to develop in the cooling system of Artis systems resulting in damage to the pump system. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Guam, 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 ARTIS ZEE AND ZEEGO, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a… The possibility exists for contaminants, in the form of biomass, to develop in the cooling system of Artis systems resulting in damage to the pump system. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Guam, 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 ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM, interventional fluoroscopic x-ray system22 AXIOM Artis, Artis… The possibility exists for contaminants, in the form of biomass, to develop in the cooling system of Artis systems resulting in damage to the pump system. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Guam, 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 Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a reusable instrument which is part of the… Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Zyston¿ Transform Instrument Case Zimmer Bioment Spine, Inc. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and Kentucky, Nevada, Pennsylvania, Tennessee, Texas, Virginia and West Virginia named
- Medical device recall Zyston¿ Transform Implant Kit Zimmer Bioment Spine, Inc. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and Kentucky, Nevada, Pennsylvania, Tennessee, Texas, Virginia and West Virginia named
- Medical device recall Invacare¿ Bariatric Bed w/o mattress & rails, Junction Boxes, Product Usage: The Invacare Bariatric home care… The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall Invacare¿ Bariatric Bed with mattress and rails , Junction Boxes, Product Usage: The Invacare Bariatric home… The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall Invacare¿ Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric… The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface… The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall Medicine Cup, 1 OZ There is 5 mL printed next to the increment on the medicine cups instead of 10 mL. The cup has the correct mL markings for the other gradations, but… Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNot namedno state, in where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system Topcon discovered an anomaly with titration, only when EpM is turned on during the titration process. Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 17, 2016ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Stratus¿ CS STAT Fluorometric Analyzer-microprocessor-controlled instrument that measures certain analytes in… Software defect, where either an Above Assay Range or an inaccurate value could potentially be reported, in the Stratus CS Acute Care Diagnostics System… Class IIFDA’s classAug 17, 2016in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedAug 17, 2016ClassClass IIStatusTerminatedWherePuerto Rico
- Medical device recall Oxylog 3000, Disposable Pediatric Patient Circuit Isolated episodes of leakage at the check valve were found FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 28 states named PublishedAug 10, 2016ClassClass IStatusTerminatedWhereNationwide, and Alaska, California, Florida, Iowa, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Hampshire, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
- Medical device recall Olympus Scientific Solutions Americas Corporation ( OSSA ) Trigger lock option does not always prevent x-ray generation. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 10, 2016ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Merge PACS software Studies coming over via telmed were missing patient’s DOB, procedure, and referring physician. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNot namedno state, in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall VITROS Immunodiagnostic Products Total T4 Reagent Pack, REF/Product Code 874 4468, Unique Identifier No.… Ortho-Clinical Diagnostics confirmed that sample results generated from VITROS Immunodiagnostic Products Total T4 Reagent Packs may show a negative bias prior… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Merge PACS software A migrated study that has annotations will display the annotations, but when a prior study is loaded that should have annotations, the second study will not… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ONLINE TDM Vancomycin 100 tests Roche Diagnostics Operations, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 50 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, 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, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall MultiDiagnost Eleva with Flat Detector The two bolts that attach the clamping plate to the lateral shaft may break, which could cause the c-arm to move laterally forward, slide out of its bearings,… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall UroDiagnost; x-ray system. Product Code: 708033 The two bolts that attach the clamping plate to the lateral shaft may break, which could cause the c-arm to move laterally forward, slide out of its bearings,… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MultiDiagnost Eleva The two bolts that attach the clamping plate to the lateral shaft may break, which could cause the c-arm to move laterally forward, slide out of its bearings,… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall AU480 Chemistry Analyzers, Reference No Beckman coulter has received complaints regarding leaking and cracked C cups. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medical device recall AU680 Chemistry Analyzers, Reference No Beckman coulter has received complaints regarding leaking and cracked C cups. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medical device recall AU5800 Chemistry Analyzers, Reference No Beckman coulter has received complaints regarding leaking and cracked C cups. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medical device recall AmediCheck Instant Test Cup Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug cup, because it may erroneously contain 12 panel cups due to a packaging error. Class IIIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedAug 10, 2016ClassClass IIIStatusTerminatedWhereNationwide, and Florida, North Carolina, Pennsylvania and Tennessee named
- Medical device recall 3T 16ch Flex SPEEDER Coil, Large, NeoCoil There is a potential for higher than specified surface temperatures involving the 3T 16ch Flex SPEEDER Large Coil. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNot namedno state, in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Synergy Cranial S7 Medtronic Navigation, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Illinois, Indiana, Massachusetts, Michigan, Missouri, North Carolina, New York, Ohio, Oregon, Texas and Utah named
- Medical device recall FrameLink. The software application is sent in CD format with an IFU, wrapped in plastic with a label for… Medtronic Navigation, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Illinois, Indiana, Massachusetts, Michigan, Missouri, North Carolina, New York, Ohio, Oregon, Texas and Utah named
- Medical device recall S7 MACH FrameLink Medtronic Navigation, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Illinois, Indiana, Massachusetts, Michigan, Missouri, North Carolina, New York, Ohio, Oregon, Texas and Utah named
- Medical device recall Synergy Spine Medtronic Navigation, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Illinois, Indiana, Massachusetts, Michigan, Missouri, North Carolina, New York, Ohio, Oregon, Texas and Utah named
- Medical device recall Fusion ENT Application Medtronic Navigation, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Illinois, Indiana, Massachusetts, Michigan, Missouri, North Carolina, New York, Ohio, Oregon, Texas and Utah named
- Medical device recall MACH Cranial Treon Medtronic Navigation, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Illinois, Indiana, Massachusetts, Michigan, Missouri, North Carolina, New York, Ohio, Oregon, Texas and Utah named
- Medical device recall MACH AxiEM Cranial Treon Medtronic Navigation, Inc. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Illinois, Indiana, Massachusetts, Michigan, Missouri, North Carolina, New York, Ohio, Oregon, Texas and Utah named
- Medical device recall RePlant¿ Angled Abutment Issue with design specification; oversized condition. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement Report23 statesnamed in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereAlabama, Arkansas, Arizona, California, Florida, Georgia, Kansas, Louisiana, Massachusetts, Michigan, Missouri, North Carolina, Nebraska, New York, Oklahoma, Oregon, South Carolina, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin
- Medical device recall TWIST DR 25X95MM Cann 12MM Thd 30MM AO Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement Report2 statesnamed in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereColorado and Illinois
- Medical device recall TWIST D 28X150MM CBS 45 Cann 14 MM AO Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement Report2 statesnamed in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereColorado and Illinois
- Medical device recall V-TEK TWIST D 3.5X90MM 30MM Can 12MM Rnd Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement Report2 statesnamed in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereColorado and Illinois
- Medical device recall V-TEK TWIST D 40X90MM 30MM Cann 12MM Rnd Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement Report2 statesnamed in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereColorado and Illinois
- Medical device recall BK Medical ApS Ultrasound System Scanner bk2300 In the system (bk3500) software generic volume measurement (HxWxLxl) function the user may be unaware of the calculation factor (1) and assume the generic… Class IIFDA’s classAug 10, 2016in FDA’s Enforcement Report3 statesnamed in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereFlorida, Massachusetts and Texas
- Medical device recall Mentor MemoryGel Breast Implant The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates. Class IIFDA’s classAug 10, 2016in FDA’s Enforcement Report11 statesnamed in where it went PublishedAug 10, 2016ClassClass IIStatusTerminatedWhereCalifornia, Colorado, Illinois, North Carolina, New Jersey, New York, Ohio, Rhode Island, Tennessee, Texas and Wisconsin
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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