Class IIOngoingZ-2177-2026
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class II recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 421–432 of 3,866 recalls
Class IIOngoingZ-2176-2026
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class IIOngoingZ-2175-2026
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class IIOngoingZ-2174-2026
Stryker Sustainability Solutions recalls BARD Dynamic Deca Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class IIOngoingZ-2173-2026
Integra LifeSciences Corp. (NeuroSciences) recalls Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.…
Out-of-specification endotoxin result that did not meet the acceptance criteria.
Integra LifeSciences C…NJMay 20, 2026
Class IIOngoingZ-2172-2026
Edwards Lifesciences, LLC recalls Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.
Edwards Lifesciences,…CAMay 20, 2026
Class IIOngoingZ-2171-2026
Aniara Diagnostica LLC recalls ZYMUTEST HIA IgG
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
Aniara Diagnostica LLCOHMay 20, 2026
Class IIOngoingZ-2170-2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces applied when the monitor is moved or rot…
PHILIPS MEDICAL SYSTEM…May 20, 2026
Class IIOngoingZ-2169-2026
Quidel Corporation recalls QuickVue Dipstick Strep A Test
Product has the potential for false positive results
Quidel CorporationCAMay 20, 2026
Class IIOngoingZ-2168-2026
Hologic, Inc recalls 3DIMENSIONS MAMMOGRAPHY SYSTEM
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
Hologic, IncMAMay 20, 2026
Class IIOngoingZ-2167-2026
Hologic, Inc recalls SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
Hologic, IncMAMay 20, 2026
Class IIOngoingZ-2166-2026
Stryker Corporation recalls Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The Flu…
Due to nonconforming products being inadvertently distributed.
Stryker CorporationCAMay 20, 2026