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Stryker Sustainability Solutions Recalls
65 recalls on record · February 27, 2013 to May 20, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
April 15, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryk
Hazard: 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.
November 19, 2025Medical DevicesFDA
Stryker Sustainability Solutions recalls HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STER
Hazard: Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.
August 28, 2024Medical DevicesFDA
Stryker Sustainability Solutions recalls Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5A
Hazard: Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing, but that may have been reprocessed, which may lead to devices not performing as intended.
July 24, 2024Medical DevicesFDA
Stryker Sustainability Solutions recalls REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Hazard: Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.