Medical devices
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2,589 medical device recalls FDA’s Enforcement Report published in 2026, the newest year, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 6, 2026.
2,589of 2,589 medical device recallsshown with your filters
The list
- Medical device recall Aquacel Ag Surgical SP Surgical dressing manufactured out of specification (greater thickness). Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 21 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, Mississippi, North Carolina, New Mexico, New York, Ohio, Pennsylvania, Tennessee, Texas and Virginia named
- Medical device recall Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS… Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if… Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedJul 15, 2026ClassClass 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 Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) OPEN HEART PEDS PACK Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) OPEN HEART PEDS PACK Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall MiniMed 780G Insulin Pump A software anomaly can occur when the pump is paired with the Instinct sensor. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall KL Owen Custom Orthodontic Solution A product error defect may cause incorrect bracket placement. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Ohio, South Carolina, Texas and Virginia named
- Medical device recall Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Due to packaging discrepancy with incorrect product size mixed up. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement Report13 statesnamed in where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereAlabama, Colorado, Iowa, Illinois, Indiana, Michigan, Montana, North Carolina, Nebraska, New York, South Dakota, Texas and Wyoming
- Medical device recall Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Due to packaging discrepancy with incorrect product size mixed up. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement Report13 statesnamed in where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereAlabama, Colorado, Iowa, Illinois, Indiana, Michigan, Montana, North Carolina, Nebraska, New York, South Dakota, Texas and Wyoming
- Medical device recall 5008X Blood Tubing Set, 24 units per case Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X… Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 24 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Illinois, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Texas and Virginia named
- Medical device recall Atellica CH Enzymatic Hemoglobin A1c (A1c_E) The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely… Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator… Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 36 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Texas, Utah, Virginia, Wisconsin and West Virginia named
- Medical device recall Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The… Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 36 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Texas, Utah, Virginia, Wisconsin and West Virginia named
- Medical device recall Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for… Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 36 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Texas, Utah, Virginia, Wisconsin and West Virginia named
- Medical device recall GSP Neonatal GALT Kit Reduction in the on-board stability of the GSP GALT assay. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 22 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, Colorado, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, New Jersey, Oregon, Puerto Rico, South Carolina, Tennessee, Texas, Virginia and West Virginia named
- Medical device recall OmniTract Surgical Retractor System, which includes 633 of the firm s The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall VITEK 2 AST-N447 TEST KIT Product reference 424620 Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall TMINI Femur Tracking Array Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Kansas, Louisiana, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, Nevada, New York, Ohio, Oregon, Pennsylvania, Texas, Utah, Virginia and Washington named
- Medical device recall Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk. Class IIFDA’s classJul 15, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 15, 2026ClassClass IIStatusOngoingWhereNationwide, and California named
- Medical device recall Breathing circuit set, coaxial Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 43 states named PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Michigan, Minnesota, Missouri, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) PAIN MGMT/ PREF W The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) BLOCK TRAY The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) MULTIMED, 7FR, 20CM, 3L, CVC BUNDLE The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) DYNJ0621189X The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) STD, INTRO-FLEX INTRODUCER 6F, C The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) IMAGING BIOPSY TRAY The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) SUTURING SET The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) SUTURE TRAY The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) ARTERIAL LINE KIT The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit) There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit) There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit) There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit) There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall Omnipod 5 Pods External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall Omnipod DASH Pod External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall Omnipod (Eros) Pod External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 8, 2026ClassClass IStatusOngoingWhereNationwide
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530B Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ901328G HEART A… Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND ARTERIAL LINE TOTE DYNJ8407 Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT… Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA - ROOM SET UP DYNJ905503D… Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
- Medical device recall Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ909090B OPEN HEART CDS QVH… Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). Class IIFDA’s classJul 8, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 8, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Illinois, Missouri, New Jersey, Ohio, Oklahoma, Tennessee, Texas and Wisconsin named
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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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