Medical devices, 2023
Shortlist up to four to read them side by side.
2,477 medical device recalls FDA’s Enforcement Report published in 2023, 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 5, 2026.
2,477of 2,477 medical device recallsshown with your filters
The list
- Medical device recall GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Glucose and Lactate Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement Report3 statesnamed in where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereMassachusetts, Minnesota and New York
- Medical device recall AVANOS BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI Certain lots of BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI were labeled as not being made with Di(2-ethylhexyl) phthalate (DEHP); however,… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations… A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Ventlab, LLC BreathTech manual resuscitators with integrated manometer, multiple accessory configurations to… A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Ventlab, LLC Horizon manual resuscitators with integrated manometer, multiple accessory configurations to… A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Ventlab, LLC RescuMed manual resuscitators with integrated manometer, multiple accessory configurations to… A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Ventlab, LLC SafeSpot manual resuscitators with integrated manometer, multiple accessory configurations to… A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Ventlab, LLC STAT-Check manual resuscitators with integrated manometer, multiple accessory configurations to… A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Ventlab, LLC V-Care manual resuscitators with integrated manometer, multiple accessory configurations to… A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Curaplex manual resuscitators with integrated manometer, multiple accessory configurations to include: 1 A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Medline manual resuscitators with integrated manometer, multiple accessory configurations to include: 1 A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 31 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, South Carolina, Tennessee, Texas, Utah, Virginia and West Virginia named
- Medical device recall Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Segmental Anchor Plug, 12 MM -For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Segmental Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Segmental Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Segmental Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Segmental Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Segmental Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 10 MM-Correction of revision of unsuccessful osteotomy, arthrodesis, or… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 12 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 16 MM- Correction of revision of unsuccessful osteotomy, arthrodesis, or… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 23 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Compress Device Short Anchor Plug, 28 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis,… Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Achieva 1.5T Potential component failure in the Gradient Coil could product smoke and/or fire. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Achieva 1.5T Conversion Potential component failure in the Gradient Coil could product smoke and/or fire. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Achieva 1.5T Initial System Potential component failure in the Gradient Coil could product smoke and/or fire. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ingenia 1.5T CX Potential component failure in the Gradient Coil could product smoke and/or fire. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Intera 1.5T Potential component failure in the Gradient Coil could product smoke and/or fire. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Intera 1.5T Power/Pulsar Potential component failure in the Gradient Coil could product smoke and/or fire. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall SmartPath to dStream for 1.5T Potential component failure in the Gradient Coil could product smoke and/or fire. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0. Poor image quality due to fluid ingress in the lens. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 49 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and 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, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall EXALT Model D Single-Use Duodenoscope, 2 pack: Outer box UPN# M00542421, Inner box UPN # M00542420 & Outer… Poor image quality due to fluid ingress in the lens. Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 49 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and 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, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning… Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Massachusetts and Tennessee named
- Medical device recall ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning… Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the… Class IIFDA’s classNov 29, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedNov 29, 2023ClassClass IIStatusOngoingWhereNationwide, and Massachusetts and Tennessee named
- Medical device recall Mobilett Mira wireless (VA20) mobile x-ray system(s) Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Class IIFDA’s classNov 22, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 22, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Atrium Advanta V12 Covered Stent System, 10mm x 59mm x 80cm (OUS)-Indicated for restoring and improving the… Balloon-to-catheter weld failure that may cause loss of balloon pressure during stent deployment. Class IIFDA’s classNov 22, 2023in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 22, 2023ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Big Bore RT with software version V4.8.0.10421 For oncology users: If the user performed off-set reconstruction on CT device a shift could be observed on the contouring area of the primary and secondary… Class IIFDA’s classNov 22, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 22, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Brilliance CT Big Bore with software version V4.8.0.10421 For oncology users: If the user performed off-set reconstruction on CT device a shift could be observed on the contouring area of the primary and secondary… Class IIFDA’s classNov 22, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 22, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Brilliance CT Big Bore Oncology with software version V4.8.0.10421 For oncology users: If the user performed off-set reconstruction on CT device a shift could be observed on the contouring area of the primary and secondary… Class IIFDA’s classNov 22, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 22, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall IBA Proton Therapy System - PROTEUS 235 The patient positioning system can perform motions in unexpected directions, creating the potential for crushing of the patient between the patient positioning… Class IIFDA’s classNov 22, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedNov 22, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Florida, Kansas and Virginia named
- Medical device recall LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051 Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class IIFDA’s classNov 22, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedNov 22, 2023ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, North Carolina, New Jersey and New York 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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