Class IIOngoingZ-0925-2026
Zimmer Surgical Inc recalls Zimmer Dermatome AN
The devices may have a misaligned thickness control bar.
Zimmer Surgical IncOHDec 24, 2025
Class II recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,501–1,512 of 3,866 recalls
Class IIOngoingZ-0924-2026
Zimmer Surgical Inc recalls Zimmer Air Dermatome
The devices may have a misaligned thickness control bar.
Zimmer Surgical IncOHDec 24, 2025
Class IIOngoingZ-0922-2026
Medline Industries, LP recalls FORCEP
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Medline Industries, LPILDec 24, 2025
Class IIOngoingZ-0921-2026
Medline Industries, LP recalls SCISSORS
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Medline Industries, LPILDec 24, 2025
Class IIOngoingZ-0920-2026
Mindray DS USA, Inc. Dba Mindray North America recalls Hardware configuration of the BeneVision Central Monitoring System (CMS)
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
Mindray DS USA, Inc. d…NJDec 24, 2025
Class IIOngoingZ-0919-2026
Stryker Medical Division Of Stryker Corporation recalls Stryker Arise 1000EX mattress
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together.…
- Alternating Pressure Air Flotation Mattress
- Release of Material/Component prior to receiving test results
Stryker Medical Divisi…MIDec 17, 2025
Class IIOngoingZ-0918-2026
Stryker Medical Division Of Stryker Corporation recalls Stryker MV3 bariatric bed
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together.…
Stryker Medical Divisi…MIDec 17, 2025
Class IIOngoingZ-0917-2026
Datascope Corp. recalls Cardiosave Rescue. Intra-Aortic Balloon Pump system.
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
Datascope Corp.NJDec 17, 2025
Class IIOngoingZ-0916-2026
Datascope Corp. recalls Cardiosave Hybrid. Intra-Aortic Balloon Pump system.
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
Datascope Corp.NJDec 17, 2025
Class IIOngoingZ-0912-2026
Nipro Medical Corporation recalls Hemodialysis System
Screw may loosen or fallout of Hemodialysis system
Nipro Medical Corporat…FLDec 17, 2025
Class IIOngoingZ-0911-2026
Medline Industries, LP recalls DEXLOCK Achilles Repair Implant Kits
There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical procedure.
Medline Industries, LPILDec 17, 2025
Class IIOngoingZ-0910-2026
Steris Corporation recalls AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description:…
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
Steris CorporationOHDec 17, 2025