Medical devices, 2012
Shortlist up to four to read them side by side.
1,310 medical device recalls FDA’s Enforcement Report published in 2012, 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.
1,310of 1,310 medical device recallsshown with your filters
The list
- Medical device recall Ventlab Rescue Med Infant Resuscitator Possible volume leakage through the inlet valve during compressions of the resuscitator bag. FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedNov 7, 2012ClassClass IStatusTerminatedWhereNationwide, and Illinois, New York, Ohio and Tennessee named
- Medical device recall AirFlow, Infant Resuscitator, AF3000 Series, Single use Possible volume leakage through the inlet valve during compressions of the resuscitator bag. FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedNov 7, 2012ClassClass IStatusTerminatedWhereNationwide, and Illinois, New York, Ohio and Tennessee named
- Medical device recall AirFlow, Small Adult Resuscitator, AF5000 Series, Single use Possible volume leakage through the inlet valve during compressions of the resuscitator bag. FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedNov 7, 2012ClassClass IStatusTerminatedWhereNationwide, and Illinois, New York, Ohio and Tennessee named
- Medical device recall West Nile Virus IgG DxSelect” kit The firm recalled due to higher reactivity with some samples in the effected lots, which may reflect a higher false positive rate. Class IIIFDA’s classNov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 7, 2012ClassClass IIIStatusTerminatedWhereNationwide
- Medical device recall Hip Components: INSERT MOBILE “COLLEGIA” TAILLE 58*28, OT22C58 There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility. Class IIFDA’s classNov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 7, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Knee Components: ROTULE “913” D=32 There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility. Class IIFDA’s classNov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 7, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility. Class IIFDA’s classNov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 7, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Software for Vitrea, Vitrea fX, and Vitrea Enterprise Suite (VES): VPMC-09293C Vitrea Vital Images has found two potential errors in calcium score values in restored snapshots of studies generated through use of Vitrea or Vitrea Enterprise Suite. Class IIFDA’s classNov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedNov 7, 2012ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall ARIA Radiation Oncology, Version 11 An anomaly has been identified with the ARIA Oncology Information System Version 11 where Monitor Units of one fraction may be incorrect, when partial… Class IIFDA’s classNov 7, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 7, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall cobas 4800 BRAF V600 Mutation Test for In Vitro Diagnostic Use Roche Molecular Systems, Inc., Product Usage:… It was identified that BRAF controls dispositioned as “Internal Use Only” were incorrectly packaged into cobas 4800 BRAF V600 Mutation Test CE-IVD kit lot… Class IIIFDA’s classNov 7, 2012in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 7, 2012ClassClass IIIStatusTerminatedWhereNo state named
- Medical device recall Reference materials “RETINAL OCT Analysis and Interpretation Method” shipped with iVue System (K091404) and… Devices labeled for an intended use not included in the existing 510(k) or PMA. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Symbiq One Channel Infuser The Symbiq pump touchscreen may not respond to user selection, may experience a delayed response, or may register a different value from the value selected by… FDA Class I, its most serious class Class IFDA’s class (needs attention)Oct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedOct 31, 2012ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Symbiq Two Channel Infuser The Symbiq pump touchscreen may not respond to user selection, may experience a delayed response, or may register a different value from the value selected by… FDA Class I, its most serious class Class IFDA’s class (needs attention)Oct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedOct 31, 2012ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall GE Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage 2.1 Seno Advantage 1.x, Seno Advantage 2.0, Seno… GE Healthcare has become aware of an issue associated with the magnification images acquired on non-GE digital mammography systems and your Seno Advantage… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 22 states named PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Kentucky, Louisiana, Massachusetts, Missouri, North Carolina, New Jersey, Nevada, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Virginia and Wisconsin named
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pulset Arterial Blood Gas (ABG) sampling kit Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Synchron Systems Synchron Calibrator Multi Calibrator Diskettes The recall was initiated because Beckman Coulter has confirmed a mislabeling error, some Synchron Systems Multi Calibrator Diskettes (REF 442600, lot M002642G)… Class IIIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIIStatusTerminatedWhereNationwide
- Medical device recall EVICEL Fibrin Sealant (Human) Ethicon and Omrix Biopharmaceuticals have received reports of air or gas embolism occuring in association with the use of spray devices employing a pressure… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall AdvanDx GNR Traffic Light PNA FISH, In Vitro Diagnostic for Culture Identification Kit for Escherichia… GNR Traffic Light PNA Fish may have false positive results with Pseudomonas putida and Pseudomonas fulva Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall GE Healthcare innova 3100, Mobile X-ray system It was discovered of a potential failure of the spectral filter mechanism inside the collimator of the innova 3100, innova 3100-IQ and innova 3131-IQ systems. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall GE Healthcare innova 3100-IQ, Mobile X-ray system The innova systems are indicated for use in generating… It was discovered of a potential failure of the spectral filter mechanism inside the collimator of the innova 3100, innova 3100-IQ and innova 3131-IQ systems. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall GE Healthcare innova 3131-IQ Mobile X-ray system It was discovered of a potential failure of the spectral filter mechanism inside the collimator of the innova 3100, innova 3100-IQ and innova 3131-IQ systems. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall AdvanDx E. coli/P. aeruginosa PNA FISH, In Vitro Diagnostic Culture Identification Kit for Escherichia coli… Some strains of Pseudomonas putida cross-react with the P. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Illinois, Michigan and New Jersey named
- Medical device recall HiRes 90K devices with Helix Electrodes Advanced Bionics is recalling the the HiRes 90K cochlear implant with HiFocus Helix Electrode because of loose-fitting insertion tool assemblies. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide, and Illinois named
- Medical device recall Oncentra External Beam 4.1 During the planning process the beam weights can be changed by the customers. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 16 states named PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, District of Columbia, Kansas, Louisiana, Missouri, North Carolina, North Dakota, New York, Ohio, Oregon, Pennsylvania, Rhode Island, South Carolina, Texas and Washington named
- Medical device recall Osseotite Tapered Certain Implant 5 X 10mm Biomet 3i recalled their Osseotite Tapered Certain Implant, Model # INT510 due to a small percentage of the devices are missing the internal threading. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement Report11 statesnamed in where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereConnecticut, Georgia, Illinois, Kansas, Massachusetts, New Hampshire, New York, Oklahoma, Oregon, Pennsylvania and Virginia
- Medical device recall The brand name of the device is Damon 3MX Bicuspid Bracket, an orthodontic bracket The firm initiated the recall as a result of a misidentification of the brackets. Class IIIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 31, 2012ClassClass IIIStatusTerminatedWhereNationwide
- Medical device recall GE Discovery NM/CT670 GE Healthcare has recently become aware of a potential safety issue associated with the table pallet of your Discovery NM/CT 670 and/or Discovery NM630 system… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 25 states named PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, Mississippi, North Carolina, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Wisconsin and West Virginia named
- Medical device recall “****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass Corporate Pkwy***4Th floor***Sunrise, FL… Ortho sensor in Sunrise, FL is recalling the Graphics User Interface Software 1.8 (which was updated to version 1.82, validated on 02/13/12). Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Michigan and New York named
- Medical device recall UniCel¿ DxC 600/800 with Software v5.0.11 Beckman Coulter has confirmed that the Shuttle to Barcode Reader and Cap Piercer alignment procedure cannot be performed on certain DxC configurations with… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement Report2 statesnamed in where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereOhio and Texas
- Medical device recall GE Healthcare, Seno Advantage 2.2 workstations with software version 22_01 and 22_02 A medical image review… GE Healthcare has recently become aware of inaccurate Scale factor annotation provided by SenoAdvantage 2.2 workstations that may impact patient safety. Class IIFDA’s classOct 31, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereNationwide, and California, Connecticut, Mississippi, New York and Texas named
- Medical device recall Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is… Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports since 2007 of various malfunctions of the power distribution and battery back-up… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement Report42 statesnamed in where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Perfusion System 8000, base 5 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is… Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports since 2007 of various malfunctions of the power distribution and battery back-up… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement Report42 statesnamed in where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Perfusion System 8000, base 4 pump, 220V/240V safety monitor included The Sarns Modular Perfusion System 8000… Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports since 2007 of various malfunctions of the power distribution and battery back-up… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement Report42 statesnamed in where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Perfusion System 8000, base 5 pump, 220V/240V safety monitor included The Sarns Modular Perfusion System 8000… Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports since 2007 of various malfunctions of the power distribution and battery back-up… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement Report42 statesnamed in where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Perfusion System 8000, base 4 pump, 100V safety monitor included The Sarns Modular Perfusion System 8000 is… Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports since 2007 of various malfunctions of the power distribution and battery back-up… Class IIFDA’s classOct 31, 2012in FDA’s Enforcement Report42 statesnamed in where it went PublishedOct 31, 2012ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin, West Virginia and Wyoming
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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