Class IIOngoingZ-2182-2026
Stryker Sustainability Solutions recalls BARD EP XT Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Ongoing recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 505–516 of 4,550 recalls
Class IIOngoingZ-2181-2026
Stryker Sustainability Solutions recalls BARD EP XT Decapolar Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class IIOngoingZ-2180-2026
Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class IIOngoingZ-2179-2026
Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class IIOngoingZ-2178-2026
Stryker Sustainability Solutions recalls BARD Dynamic XT Deca Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
Class IIOngoingZ-2177-2026
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable
Incomplete seals on sterile product
Stryker Sustainability…AZMay 20, 2026
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Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.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