Fresh Recalls

Stryker Sustainability Solutions recalls

33 recent recalls on record for Stryker Sustainability Solutions in connected official government data as of October 22, 2026 at 12:00 PM UTC.

Models with recalls

BARD Dynamic Deca Steerable (1)BARD Dynamic Tip Steerable (3)BARD Dynamic XT Deca Steerable (1)BARD Dynamic XT Steerable (2)BARD EP XT Decapolar Steerable (2)BARD EP XT Steerable (1)BW Webster Duo-Decapolar (1)CS Uni-Directional w Auto ID (2)Daig Livewire Steerable (12)Daig Livewire Steerable BDB (1)Medtronic Marinr Steerable (1)REF (6)

All Stryker Sustainability Solutions recalls

FDA Class II · Medical device · October 14, 2026

BARD EP XT DECAPOLAR STEERABLE recall — Stryker Sustainability Solutions

Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to particulate embolization,…

Official ID Z-0085-2027 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Official ID Z-3187-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Official ID Z-3186-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Official ID Z-3185-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Official ID Z-3184-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Official ID Z-3183-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Official ID Z-3182-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Medtronic Marinr Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2199-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable BDB recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2198-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2197-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2196-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2195-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2194-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2193-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2192-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2191-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2190-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2189-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2188-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2187-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Daig Livewire Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2186-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

CS Uni-Directional w Auto ID recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2185-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

CS Uni-Directional w Auto ID recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2184-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BW Webster Duo-Decapolar recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2183-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD EP XT Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2182-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD EP XT Decapolar Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2181-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD Dynamic XT Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2180-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD Dynamic XT Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2179-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD Dynamic XT Deca Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2178-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD Dynamic Tip Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2177-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD Dynamic Tip Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2176-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD Dynamic Tip Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2175-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD Dynamic Deca Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Official ID Z-2174-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.