Medical devices, 2014
Shortlist up to four to read them side by side.
3,059 medical device recalls FDA’s Enforcement Report published in 2014, 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.
3,059of 3,059 medical device recallsshown with your filters
The list
- Medical device recall 6.5 mm Cancellous Screw Fully Threaded Sterile zimmer Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report45 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arizona, California, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Virginia, US Virgin Islands, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall 4.5 mm Malleolar Screw Sterile zimmer Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report45 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arizona, California, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Virginia, US Virgin Islands, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall 4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report45 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arizona, California, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Virginia, US Virgin Islands, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Philips IntelliSpace PACS 4.4 image management systems performs digital image processing, measurement and… A problem was detected in the Philips IntelliSpace PAC 4.4 software where if patient information is changed in the DICOM header and the study is exported… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Pivot Bipolar Cup 22x42/43-51/53mm Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Patella 38mm, REF164-0038 Product Usage: UHMWPE component used in a TKA procedure to resurface the patella… Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall PS Tibial Insert Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Tibila Insert UC, Balanced Knee System, REF163-3YYY Product Usage: UHMWPE component used in TKA procedures to… Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Tibila Insert CK, Balanced Knee System Revision, REF563-1YYY Product Usage: UHMWPE component used in TKA and… Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL, 125o There was an error in manufacturing which resulted in the proximal lag screw hole being positioned incorrectly in several batches of TRIGEN(R); INTERTAN(TM);… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Medtronic, Activa PC Medtronic is recalling six Activa PC (model 37601) Implantable Neurostimulators due to the potential for a damaged electrical component during manufacturing. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereMassachusetts, North Carolina, Ohio and Texas
- Medical device recall Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 10 cm Infusion Pattern AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long). Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 30 cm Infusion Pattern AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long). Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 40 cm Infusion Pattern AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long). Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall WaterLase iPlus Dental Laser System Biolase is recalling the WaterLase iPlus Dental Laser System because of a discrepancy present in the user interface software (version 1.7). Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall All brochures printed before November 20, 2013 for the HyperBlue 1530 medical laser, including the product… Brochures and web site information for the HyperBlue 1530 diode laser promoted features which had not been cleared in the product’s premarket notification to… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report10 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereColorado, Florida, Georgia, Maryland, Missouri, Ohio, Pennsylvania, Texas, Utah and Washington
- Medical device recall Synthes 3.0 MM TI Cannulated Screw Instrument and Implant Set A screw set was returned from the field for destruction after being exposed to flood water, which was erroneously reprocessed and returned to the field. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report2 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereMichigan and Wisconsin
- Medical device recall Gelweave (TM) Vascular Prostheses The cautery that is provided with the Gelweave graft in the box has a shorter shelf life indicated on its label, versus that of the graft (4 years and 5 years,… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 47 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, 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, Washington, Wisconsin and West Virginia named
- Medical device recall IntelePACS software versions 3-8-1 to 4-9-1, Product Usage: IntelePACS is a device that receives digital… In specific situation a partially truncated file may be written to the IntelePACS server. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor system The blood pressure (BP) circuit occasionally fails to inflate the blood pressure cuff and the BP circuit fails to activate, resulting in no BP measured. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Gyrus ACMI Falope-Ring Dilator, item 000878-4 Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold as a stand-alone non-sterile component. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 27 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Louisiana, Maryland, Michigan, Minnesota, Mississippi, New Hampshire, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller… The wireless function of the IP5 radio could be interrupted causing loss of wireless communication between the IP5 and host monitoring system. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Units may be labeled with the incorrect diopter power. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray, non-sterile The intended use of the… The firm discovered that the current Personal Tibial/General Fixed Bracket Trays may not have the specific geometry to accommodate the tibial drill and stop… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report18 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereArizona, California, Colorado, Florida, Illinois, Indiana, Kansas, Michigan, Minnesota, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas and Virginia
- Medical device recall PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray, non-sterile The intended use of the… The firm discovered that the current Personal Tibial/General Fixed Bracket Trays may not have the specific geometry to accommodate the tibial drill and stop… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report18 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereArizona, California, Colorado, Florida, Illinois, Indiana, Kansas, Michigan, Minnesota, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas and Virginia
- Medical device recall PENTAX Upper/Lower G.I The Instructions for Use for the Pentax OF-B130 and OF-B194 Gas/Water Valve IFU if not followed carefully may cause a potential risk to health. Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report5 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereCalifornia, Colorado, Idaho, Indiana and Kansas
- Medical device recall GE Healthcare, Discovery XR656P/N 5374989/5397837 is intended to generate digital radiographic images of the… GE Healthcare has become aware of a potential safety issue involving the nylon hooks which support the FlashPad” detector on the Discovery XR656 wall stand… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement Report31 statesnamed in where it went PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Colorado, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Louisiana, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, New Jersey, New Mexico, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia
- Medical device recall CAP Change Kit w/MicroClave Clear ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama and Maryland named
- Medical device recall Cap Change Kit with MicroClave Clear Connector ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama and Maryland named
- Medical device recall Port Access Kit with MicroClave Clear Connector ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility… Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama and Maryland named
- Medical device recall Persona (TM) The Personalized Knee System PS Tibial Articular Surface Provisional Top Nonsterile TASP PS L… Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 44 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and Wyoming named
- Medical device recall Persona (TM) The Personalized Knee System Tibial Articular Surface Provisional Bottom Nonsterile TASP L CD… Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). Class IIFDA’s classAug 27, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 44 states named PublishedAug 27, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin 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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