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 7, 2026.
3,394of 3,394 medical device recallsshown with your filters
The list
- Medical device recall TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dislocation The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall 3M Durapore Surgical Tape Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were incorrectly labeled with a shelf life of 5 years, rather than 3 years. Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Georgia, Illinois, Maryland, North Carolina, New Hampshire, New York, Texas and Virginia named
- Medical device recall Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch Products may not be heparin coated as indicated on the label-leads to a potential loss of benefit due to the absence of the heparin coating Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch Products may not be heparin coated as indicated on the label-leads to a potential loss of benefit due to the absence of the heparin coating Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall QUIDEL InflammaDry MMP-9 Test There are two windows on the test device, the control line window and the test results window. Class IIFDA’s classMay 1, 2024in FDA’s Enforcement Report44 statesnamed in where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall QUIDEL InflammaDry MMP-9 Test There are two windows on the test device, the control line window and the test results window. Class IIFDA’s classMay 1, 2024in FDA’s Enforcement Report44 statesnamed in where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide, and Illinois and Texas named
- Medical device recall Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide, and Illinois and Texas named
- Medical device recall Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide, and Illinois and Texas named
- Medical device recall Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK Product was distributed in the United States without proper regulatory approval. Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Georgia, Indiana, Louisiana, New York and Virginia named
- Medical device recall Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1 Possible failure of Uninterruptable Power Supply (UPS) devices supporting the Patient Information Center (PIC) iX system, potential for the associated PIC iX… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System Elekta has become aware that Disposable Biopsy Needles (911933) from one batch (837838839) can contain some microscopic debris on the inside of the biopsy… FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNo state named
- Medical device recall Tablo Hemodialysis System Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing, with less than 336 hours usage, will be replaced because tubing may contain… FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement Report42 statesnamed in where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, District of Columbia, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Aeris EVO, all software versions except 1.05.06.00 Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Garbin EVO, all software versions except 1.05.06.00 Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall LifeVentEVO2, all software versions except 1.05.06.00 Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Trilogy EV300, all software versions except 1.05.06.00 Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Trilogy Evo O2, all software versions except 1.05.06.00 Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Trilogy Evo, all software versions except 1.05.06.00 Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00 Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall Dr¿ger Perseus A500 Anesthesia Workstation Unexpected shutdown while operating on battery power. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereNationwide
- Medical device recall AW-S025 NEO SONARMED SENSOR 2.5MM The failure to detect the partial obstruction in a 2.5mm sensor. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement Report19 statesnamed in where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereAlaska, Arizona, California, Florida, Illinois, Kentucky, Maryland, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia and Washington
- Medical device recall AW-S030 NEO SONARMED SENSOR 3.0MM The failure to detect the partial obstruction in a 2.5mm sensor. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement Report19 statesnamed in where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereAlaska, Arizona, California, Florida, Illinois, Kentucky, Maryland, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia and Washington
- Medical device recall AW-S035 NEO SONARMED SENSOR 3.5MM The failure to detect the partial obstruction in a 2.5mm sensor. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement Report19 statesnamed in where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereAlaska, Arizona, California, Florida, Illinois, Kentucky, Maryland, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia and Washington
- Medical device recall Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical… The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal… Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical… The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal… Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical… The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal… Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Chiba Biopsy Needle - Used for aspiration biopsy Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for… Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Yueh Centesis Disposable Catheter Needle - Intended for use in percutaneous fluid aspirations, such as… Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Peel-Away Introducer - Intended for the percutaneous introduction of balloon, electrode and closed or… Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for anchoring the anterior wall of the… Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Dilator - Intended to be used for dilating puncture sites or catheter tracts for percutaneous placement of… Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Dilator With AQ Hydrophilic Coating - Intended to be used for dilating puncture sites or catheter tracts for… Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Dilator - Coons Taper - Used for dilating puncture sites or catheter tracts for percutaneous placement of… Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device: STRATAFIX SPIRAL MONOCRYL PLUS… Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility Class IIFDA’s classApr 24, 2024in FDA’s Enforcement Report9 statesnamed in where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereColorado, Georgia, Iowa, Michigan, New Jersey, New York, Pennsylvania, South Carolina and Wisconsin
- Medical device recall POLYSIN (Polyglycolic Acid) suture, HSM9 5-0 BR PGA Complaints have been received with allegations of Incorrect Needle Curvature. Class IIFDA’s classApr 24, 2024in FDA’s Enforcement Report9 statesnamed in where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereArizona, California, Illinois, Massachusetts, Maryland, Minnesota, New Jersey, Pennsylvania and Texas
- Medical device recall AW-M0001 SONARMED MONITOR Software anomaly resulted in failure to detect a partial obstruction in 2.5 mm sensors and up to 3mm distal to the sensor. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement Report19 statesnamed in where it went PublishedApr 24, 2024ClassClass IStatusOngoingWhereAlaska, Arizona, California, Florida, Illinois, Kentucky, Maryland, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia and Washington
- Medical device recall Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor) Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring. Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Masimo Rad-G, Pulse Oximeter (W/Sensor) Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring. Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Masimo Rad-G, Pulse Oximeter (W/Patient Cable) Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring. Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Masimo Rad-G, Pulse Oximeter (W/Patient Cable) Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring. Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Smiths Medical Medfusion Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and… Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Smiths Medical Medfusion Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and… Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Smiths Medical Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and… Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Smiths Medical Medfusion Guide Barrel Clamp Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and… Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 24, 2024ClassClass IIStatusOngoingWhereNo state 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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