Medical devices, 2022
Shortlist up to four to read them side by side.
2,192 medical device recalls FDA’s Enforcement Report published in 2022, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 5, 2026.
2,192of 2,192 medical device recallsshown with your filters
The list
- Medical device recall Canon Aplio ultrasound system After completion, ultrasound system’s Stress Echo may not terminate if user does not manually terminate the protocol. Class IIFDA’s classNov 16, 2022in FDA’s Enforcement Report23 statesnamed in where it went PublishedNov 16, 2022ClassClass IIStatusOngoingWhereArkansas, California, Colorado, Florida, Georgia, Iowa, Illinois, Kansas, Kentucky, Louisiana, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, New York, Oklahoma, Pennsylvania, South Carolina, Tennessee, Washington and West Virginia
- Medical device recall Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserted Central Catheter Scalpel and StatLock components packaged with specific lots of the HydroPICC catheter have a shorter expiration date than what is listed on the outer kit… Class IIFDA’s classNov 16, 2022in FDA’s Enforcement Report4 statesnamed in where it went PublishedNov 16, 2022ClassClass IIStatusTerminatedWhereIllinois, North Carolina, New Jersey and Rhode Island
- Medical device recall VITROS Chemistry Products Calibrator Kit 9 -(GEN) 22 of VITROS PHYT Slides For in vitro diagnostic use only Calibration disk Data Release Version (DRV) 6194 to 6200 contain inappropriate calibration mathematics for VITROS Calibration Kit 9 for calibrating VITROS PHYT… Class IIFDA’s classNov 16, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 16, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark… Product missing one of two welds connecting the tip to the shaft, if the remaining weld breaks, it is possible that the tip could fall out during X-Mark… Class IIFDA’s classNov 16, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 16, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall NEO-fit Neonatal Endotracheal Tube Grip Firm has received 11 complaints involving a loose or detached metal clips, including 3 cases where the metal clip was ingested by the patient, and 3 cases… Class IIFDA’s classNov 16, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedNov 16, 2022ClassClass IIStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal endoscopic procedures for… ***Update12/13/22***:Product removal due to higher incidence of adverse events of foreign body reactions*** Potential outcomes associated with foreign body… Class IIFDA’s classNov 16, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 16, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use in gastrointestinal endoscopic procedures… ***Update12/13/22***:Product removal due to higher incidence of adverse events of foreign body reactions*** Potential outcomes associated with foreign body… Class IIFDA’s classNov 16, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 16, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal… ***Update12/13/22***:Product removal due to higher incidence of adverse events of foreign body reactions*** Potential outcomes associated with foreign body… Class IIFDA’s classNov 16, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 16, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Hillrom Centrella Hospital Bed with WatchCare Incontinence Management System Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 9, 2022in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 9, 2022ClassClass IStatusOngoingWhereNo state named
- Medical device recall Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Centrella Bed Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 9, 2022in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 9, 2022ClassClass IStatusOngoingWhereNo state named
- Medical device recall Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Progressa Bed Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 9, 2022in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 9, 2022ClassClass IStatusOngoingWhereNo state named
- Medical device recall Hillrom Hospital Bed Accessory, WatchCare Incontinence Management System for VersaCare Bed Rev Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 9, 2022in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 9, 2022ClassClass IStatusOngoingWhereNo state named
- Medical device recall Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for VersaCare Bed Rev Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 9, 2022in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 9, 2022ClassClass IStatusOngoingWhereNo state named
- Medical device recall Fogarty Arterial Embolectomy Catheters Due to an increase of confirmed latex deterioration complaints for arterial embolectomy catheters packaged in pouches. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedNov 9, 2022ClassClass 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, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Fogarty Biliary Balloon Probes Due to an increase of confirmed latex deterioration complaints for arterial embolectomy catheters packaged in pouches. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedNov 9, 2022ClassClass 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, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin Weak skin adhesion. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 9, 2022ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall EKOS Control Unit 4.0 console, a component of the EKOS Control System 4.0, which is a component of the… Consoles were shipped without an instruction for use (IFU) or with the incorrect IFU. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report7 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereCalifornia, Illinois, Kentucky, Ohio, Oklahoma, Rhode Island and Texas
- Medical device recall STRATAFIX SPIRAL PGA-PCL UNI UD 20CM USP2-0(M3) S/A SH Packages may contain a PS-1 cutting edge needle and not the intended SH taper point needle may result in more tissue trauma than is anticipated for taper point… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNo state named
- Medical device recall EMBLEM S-ICD, Subcutaneous Implantable Defibrillators There is an incorrect manufacturing date/timestamp within the software which causes an inaccurate display of battery capacity. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall EMBLEM MRI S-ICD, Subcutaneous Implantable Defibrillator There is an incorrect manufacturing date/timestamp within the software which causes an inaccurate display of battery capacity. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall CritiCool, thermoregulation device Premature pump failure may lead to the device displaying a HALT 4 error, from which the device cannot recover even after device reboot. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BAUSCH + LOMB EYE PACK Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall BAUSCH + LOMB PHACO PACK Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall BAUSCH + LOMB BASIC OPHTHALMIC PACK Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall BAUSCH + LOMB CATARACT PACK Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall BAUSCH + LOMB EYE MUSCLE Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall BAUSCH + LOMB CATARACT TRAY Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall BAUSCH + LOMB CATARACT PACK Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall MEDLINE LITHOTOMY Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall MEDLINE LINQ TRAY Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall MEDLINE DENTAL PACK Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall MEDLINE RADIOLOGY PROCEDURE PACK Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall MEDLINE CVC BARRIER KIT Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Minnesota, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee and Texas named
- Medical device recall Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of… Unable to charge the battery pack- battery packs will allow the batteries to be charged if the voltage of any cell is below 2.5V. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide
- Medical device recall THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter Manufacturing error resulted in potential contamination of Bi-Directional navigation catheter irrigation path with cellulose fibers that can cause 1) Failure… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and Colorado, Florida, Georgia, Illinois, Michigan, Missouri, North Carolina, New Jersey, Ohio, Oregon, South Dakota, Tennessee, Texas, Virginia and Wisconsin named
- Medical device recall WEB Detachment Controller Detachment controller, of an aneurysm embolization system, has an out of specification tunnel opening dimension, which may prevent the implant device pusher… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement ReportNationwideFDA’s word, and 17 states named PublishedNov 9, 2022ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Illinois, Indiana, Kansas, Louisiana, Michigan, Minnesota, North Carolina, Nebraska, New York, Ohio, Pennsylvania, Tennessee, Texas, Utah and Virginia named
- Medical device recall BD Trucount Tubes (Cat Due to partial label detachment on tubes. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report43 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington and Wisconsin
- Medical device recall BD Trucount Tubes (Cat Due to partial label detachment on tubes. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report43 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington and Wisconsin
- Medical device recall BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat Due to partial label detachment on tubes. Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report43 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington and Wisconsin
- Medical device recall BD Nexiva Closed IV Catheter System - Single Port During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report13 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusOngoingWhereFlorida, Georgia, Illinois, Massachusetts, Maryland, Maine, North Carolina, New Jersey, New York, Pennsylvania, Rhode Island, South Carolina and Virginia
- Medical device recall Allen Advance Table, RSP-ADVANCE TABLE: a) the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report4 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusTerminatedWhereMichigan, Texas, Washington and Wisconsin
- Medical device recall C-Flex Polar Head Positnr-Device Only, SSP-NEUROSURGICAL HEADREST the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report4 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusTerminatedWhereMichigan, Texas, Washington and Wisconsin
- Medical device recall Allen Standard Starburst, Mayfield/Doro, STANDARD SPINE POSITIONERS CMPT the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report4 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusTerminatedWhereMichigan, Texas, Washington and Wisconsin
- Medical device recall Beach Chair Clamp, BEACH CHAIR SHLDER POSITIONER CMPT the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report4 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusTerminatedWhereMichigan, Texas, Washington and Wisconsin
- Medical device recall Allen Life Assist Beach Chair, BCSSP-BEACH CHAIR the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report4 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusTerminatedWhereMichigan, Texas, Washington and Wisconsin
- Medical device recall Simple Clamp, US/EURO Rails, UPPER EXTREMITY DISTRACTION CMPT the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and… Class IIFDA’s classNov 9, 2022in FDA’s Enforcement Report4 statesnamed in where it went PublishedNov 9, 2022ClassClass IIStatusTerminatedWhereMichigan, Texas, Washington and Wisconsin
- Medical device recall AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Due to increase in Li-Ion Battery failures Class IIFDA’s classNov 2, 2022in FDA’s Enforcement Report48 statesnamed in where it went PublishedNov 2, 2022ClassClass IIStatusOngoingWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, 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, Texas, Utah, Virginia, US Virgin Islands, Vermont, Washington, Wisconsin, West Virginia and Wyoming
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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