Medical devices, 2017
Shortlist up to four to read them side by side.
2,615 medical device recalls FDA’s Enforcement Report published in 2017, 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.
2,615of 2,615 medical device recallsshown with your filters
The list
- Medical device recall Cataract Kit - Dr AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Cataract Pack AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Custom Tray, part numbers PSS1111 and PSS1111(A. Product packaged in a convenient manner for use in a general… AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Dicken Eye Pack AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A Product packaged in a convenient manner for use in a… AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall ENT Pack, part number AMS2727 Product packaged in a convenient manner for use in a general clinical procedure AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Eye Cataract Pack AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general… AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical… AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Minor Operation Kit AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Ophthalmic Pack AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Ortho Basic Pack AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Plastic Pack AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall PRK Tray, part number DDS1044 Product packaged in a convenient manner for use in a general clinical procedure AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Setup Pack, part number AMS3112(A Product packaged in a convenient manner for use in a general clinical… AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Vitrectomy Kit AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall Vitrectomy Pack AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Iowa, Kentucky, Massachusetts, Minnesota, Missouri, North Dakota, New Jersey, Nevada, Ohio, South Dakota, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall VIDAS Estradiol II Fulvestrant cross reacts with the VIDAS Estradiol II immunoassay and may cause falsely elevated estradiol results in patients treated with Fulvestrant. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Colorado, Florida, Georgia, Iowa, Indiana, Louisiana, Michigan, Mississippi, North Carolina, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Texas and Washington named
- Medical device recall Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Lower Back Garment Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep penetrating heat garment and wraps During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use… Aesculap Implant Systems LLC is recalling the Minop Trocar due to the possibility it may have sharp edges on the distal end which may lead to the abrasion of… Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Radiation Therapy Treatment Planning System An error in NVIDIA GPU (Graphics Processing Unit) card drivers can occur for certain software programs. Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 34 states named PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Illinois, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Mississippi, Montana, North Carolina, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, Tennessee, Texas, Virginia, US Virgin Islands, Vermont, Washington and Wisconsin named
- Medical device recall TotalCare Bed Systems The bed exit alarm may not function properly if the alarm has been armed for a period longer than seventy-two (72) hours without the alarm being triggered by… Class IIFDA’s classApr 19, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Nordson Micromedics FibriJet Endoscopic Catheter Introducer The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package integrity may be compromised which may… Class IIFDA’s classApr 19, 2017in FDA’s Enforcement Report9 statesnamed in where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Mississippi, North Carolina, New Jersey, New York, Tennessee and Texas
- Medical device recall Keystone Dental Inc Straight PrimaConnex Implants contained Tapered PrimaConnex Implants Class IIFDA’s classApr 19, 2017in FDA’s Enforcement Report9 statesnamed in where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereCalifornia, Florida, Illinois, Indiana, Massachusetts, Minnesota, New Jersey, Nevada and Pennsylvania
- Medical device recall da Vinci Xi EndoWrist Suction Irrigator, 8 mm instrument Intuitive Surgical has become aware that in specific scenarios with system software P6 and the da Vinci Xi Suction Irrigator (PN 480299-03), users can… Class IIFDA’s classApr 19, 2017in FDA’s Enforcement Report6 statesnamed in where it went PublishedApr 19, 2017ClassClass IIStatusTerminatedWhereAlabama, Colorado, Kansas, Nevada, New York and Texas
- Medical device recall Beckman Coulter Chemistry Analyzer AU680/AU5800 Beckman Coulter is recalling the Rack ID Labels because the Rack ID number displayed and the Rack ID barcode label do not match. Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportMassachusettsthe one state its words name PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereMassachusetts
- Medical device recall The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein. Arrow International, Inc. Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Mobile Diagnostic X-Ray System with Digital Panel When the operator moves an image to another view then the electronic marker might be placed at the wrong anatomical position in the resulting image. Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, North Carolina, New Mexico, New York, Ohio, Oregon, Pennsylvania, South Carolina, Texas, Vermont and Wisconsin named
- Medical device recall Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352 Exchange part (service numbers):… Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically switch to Monitor Mode with audible alarms when association with central monitoring… Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall eCare Coordinator Product Usage: is software intended for use in data aggregation, patient interaction… eCareCoordinator (eCC) is intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent… Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Access 2 Immunoassay Systems Beckman Coulter is recalling the Access 2 Family of Immunoassay Systems because a circuit board that controls motor functions can affect device positioning on… Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedApr 12, 2017ClassClass IIStatusTerminatedWherePuerto Rico
- Medical device recall Access 2 assay Immunoassay System, Remanufactured Beckman Coulter is recalling the Access 2 Family of Immunoassay Systems because a circuit board that controls motor functions can affect device positioning on… Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedApr 12, 2017ClassClass IIStatusTerminatedWherePuerto Rico
- Medical device recall UniCel DxC 600i SYNCHRON Access Clinical System Beckman Coulter is recalling the Access 2 Family of Immunoassay Systems because a circuit board that controls motor functions can affect device positioning on… Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedApr 12, 2017ClassClass IIStatusTerminatedWherePuerto Rico
- Medical device recall ADVIA Chemistry Enzyme 2 Calibrator, multi-analyte mixture Product Usage: Assays included in Enzyme 2… Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in quality control and patient results for Aspartate Aminotransferase (AST) and… Class IIIFDA’s classApr 12, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 12, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medical device recall NucliSENS Lysis Buffer Problem with colored eluates for whole blood extractions Class IIFDA’s classApr 12, 2017in FDA’s Enforcement Report3 statesnamed in where it went PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereIllinois, Ohio and Washington
- Medical device recall STAPLER,IS4000 Intuitive Surgical has become aware and further investigation has determined that misinterpretation of instructions provided on the IS4000 Stapler Release Kit… Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall STAPLER,IS4000 Intuitive Surgical has become aware and further investigation has determined that misinterpretation of instructions provided on the IS4000 Stapler Release Kit… Class IIFDA’s classApr 12, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 12, 2017ClassClass IIStatusTerminatedWhereNationwide
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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