Vehicle Safety
Recalls Search 320,000+ NHTSA safety recalls Complaints 2.1M+ consumer safety complaints TSBs 4.7M technical service bulletins VIN Lookup Decode any vehicle VIN instantly OBD Codes 12,000+ diagnostic trouble codes Fuel Economy EPA MPG data for all vehicles Statistics Recall trends & safety analysis
Consumer Safety
Product Safety 9,700+ CPSC product recalls Food Safety 28,600+ FDA food recalls Pet Safety 1.3M FDA animal adverse events Drug Safety 17,500+ FDA drug recalls Device Safety 38,400+ FDA device recalls Workplace Safety 102,900+ OSHA injury reports
Infrastructure
Bridge Safety 624,000 bridge inspections Aviation Safety 30,000+ NTSB aviation events Dam Safety 92,600 dam safety records Water Safety 433,000+ public water systems Railroad Safety 438,000+ rail crossings Pipeline Safety 8,800+ pipeline incidents
Public Health
Nursing Homes 14,700 CMS rated facilities Environmental 80,000+ hazardous sites & releases

Browse Device Recalls

6 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 6 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Medical Device Recalls

Browse 6 FDA device recalls.

Clear
DateProductReasonClassFirm
Aug 2, 2024 Monarch Platform (Urology), REF: MON-000007, MON-000007-RFB Endoscopy/bronchoscopy/urology devices may have a strain relief defect with some cart and tower p... Class II AURIS HEALTH INC
Aug 2, 2024 Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch ... Endoscopy/bronchoscopy/urology devices may have a strain relief defect with some cart and tower p... Class II AURIS HEALTH INC
Oct 18, 2023 Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w Their is the potential that software issues may result in flipped image of the virtual Bronchosc... Class II AURIS HEALTH INC
Oct 18, 2023 Monarch Platform REF MON-000005-01R, 100-240V- 50/60Hz 1440w Their is the potential that software issues may result in flipped image of the virtual Bronchosc... Class II AURIS HEALTH INC
Oct 18, 2023 Monarch Platform REF MON-000006 100-240V- 50/60Hz 1440w Their is the potential that software issues may result in flipped image of the virtual Bronchosc... Class II AURIS HEALTH INC
Apr 19, 2019 Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120 Reports of aspirating biopsy needle breakage Class II AURIS HEALTH INC

Frequently Asked Questions

When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.

All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.

Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.