Medical devices, 2024
Shortlist up to four to read them side by side.
3,394 medical device recalls FDA’s Enforcement Report published in 2024, 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.
3,394of 3,394 medical device recallsshown with your filters
The list
- Medical device recall Alinity hq Analyzer 1)If Complete Blood Count with differential and reticulocyte(CBC+Diff+Retic) sample is run, then immediately following on same rack CBC+Diff sample is run,… Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and North Carolina, New York and Oklahoma named
- Medical device recall BIOFIRE FILMARRAY Pneumonia Panel Pneumonia panels have an increased risk of control failures due to an issue in the manufacturing process, which could lead to delayed results for the customer. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Alabama, Indiana and West Virginia named
- Medical device recall BIOFIRE FILMARRAY Pneumonia Panel plus Pneumonia panels have an increased risk of control failures due to an issue in the manufacturing process, which could lead to delayed results for the customer. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Alabama, Indiana and West Virginia named
- Medical device recall The VITROS XT Chemistry Products ALB-TP Slides is a single device that contains both an albumin test and a… The reason for this recall is QuidelOrtho has determined that during normal use the VITROS XT ALB-TP Slides may shed dust and debris as they travel through the… Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Regard Kit containing the Microtek decanter Decanters may have pin holes and tears in sterile packaging that cannot be identified visually. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Missouri named
- Medical device recall BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for susceptibility testing of Mycobacterium… May intermittently produce falsely resistant results for pyrazinamide (PZA) during susceptibility testing of Mycobacterium tuberculosis isolates. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Arizona, Florida, Georgia, Illinois, Louisiana, Maryland, Michigan, Minnesota, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, Texas, Utah and Washington named
- Medical device recall Barricaid Annular Closure Impactor At least two units have been found to be missing a weld. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Disposable 5 Lead Cable and Lead Wire System, 50 inches Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain,… Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 12 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Colorado, Florida, Louisiana, Michigan, Mississippi, Oregon, Tennessee, Texas, Wisconsin and Wyoming named
- Medical device recall DxC 500 AU Clinical Chemistry Analyzer Due to a software issues, after the instrument processes 250 racks cumulatively, any subsequent racks with samples requiring rerun/reflex will be held in the… Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 13 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Alabama, California, Georgia, Hawaii, Illinois, Michigan, Minnesota, Mississippi, Nebraska, New York, Oregon, Pennsylvania and South Carolina named
- Medical device recall IBA Proton Therapy System - PROTEUS 235- Designed to produce and deliver a proton beam for the treatment of… Temporary deactivation of collision detection for Forte Robotic Patient Positioning System occasionally experiences issues Class IIFDA’s classAug 28, 2024in FDA’s Enforcement Report9 statesnamed in where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereIllinois, Louisiana, Michigan, New Jersey, Oklahoma, Tennessee, Texas, Virginia and Washington
- Medical device recall LINER, SOFT, SUCTION CANISTER, 1500CC A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall LINER, SOFT, SUCTION CANISTER, 1500CC A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall 1500ML SOFT LINER, 1/4X6 TBG NS A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall 1,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall 1,5L MED-SOFT LINER W/ 6MMX3M TUB. & ADULT VC A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall 1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT ADULT A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET UP A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: DENTAL A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) BASIC NASAL A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) CYSTO A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) ENDO KIT A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) ENDO KIT A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) MAJOR BREAST A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) AAA CDS A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) TURNOVER KIT A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) BASIC NEURO A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) GYN CDS A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) C-SECTION CDS A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline medical procedure kits labeled as follows: a) ARTHROSCOPY A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall GM60A. Digital Diagnostic Mobile X-Ray System. Potential for the anti-fall system of the device arm to fail. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Connecticut, District of Columbia, Georgia, Indiana, Kansas, Massachusetts, Maryland, Missouri, Mississippi, North Carolina, North Dakota, New Jersey, Nevada, Ohio, Pennsylvania, Virginia and West Virginia named
- Medical device recall Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional Fluoroscopic X-Ray System A half-threaded bolt was included in the LTE kits instead of the correct full-threaded bolt. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Illinois and Oregon named
- Medical device recall Covideien McGRATH MAC Video Laryngoscope IFU update to address device’s battery handling information. Class IIFDA’s classAug 28, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 53 states named PublishedAug 28, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, US Virgin Islands, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Orthopantomograph OP300 dental computed tomography x-ray system It was noticed in production on 28.10.2021, that the final testing database gives a pass result for Pan ADC repeatability test even when the test result is not… Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010 Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected… FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 21, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum A+ & Plum A+3 Infusion Systems, Pump… Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected… FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 21, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Plum 360/A+ spare batteries Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected… FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 21, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall RMU-2000 Automated Chest Compression Device Problem in the device’s motor may cause the device to stop compressions. FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 21, 2024in FDA’s Enforcement Report5 statesnamed in where it went PublishedAug 21, 2024ClassClass IStatusOngoingWhereConnecticut, Florida, New Jersey, South Carolina and Tennessee
- Medical device recall Beckman Coulter DxI 9000 Access Immunoassay Analyzer The reason for this recall is Beckman Coulter has determined that when a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory Automation System… Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Georgia, Indiana, Kansas, Maine, New Hampshire, New Jersey, Oklahoma, Pennsylvania and Texas named
- Medical device recall Discrete photometric chemistry analyzer for clinical use. Beckman Coulter, Inc. Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and Alabama, California, Illinois, Louisiana, Michigan, Montana, Nebraska, New York and Texas named
- Medical device recall Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classAug 21, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedAug 21, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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