Stryker
37 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Stryker and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-05-20FDA-DeviceClass IIMedtronic Marinr catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIDaig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheters recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker electrophysiology catheter recalled for seal defect
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker electrophysiology catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker electrophysiology catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD EP XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD EP XT catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD Dynamic XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD Dynamic XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD Dynamic XT catheters recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD Dynamic Tip Steerable recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceClass IIStryker FluidSmart Urology Tube Set recalled for manufacturing defect
Due to nonconforming products being inadvertently distributed.
- 2026-04-15FDA-DeviceClass IIStryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (Red) Dual Port Single Bladder REF 5921-018-235.
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
- 2026-04-08FDA-DeviceClass IICheck Stryker CHROMOPHARE surgical light ceiling support
Surgical light assembly may not adequate support the weight of the ceiling cover.
- 2026-03-25FDA-DeviceClass IICheck your Stryker Cub crib serial number
Cribs sold in the USA are missing two access door warning labels.
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