BARD EP XT Decapolar Steerable: recall status

⚠ Recalls found. BARD EP XT Decapolar Steerable is named in 2 official recalls in our current data:

FDA Class II recall Z-0085-2027 — 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, infection, thrombus or ganuloma formation from particulate matter.
FDA Class II recall Z-2181-2026 — Incomplete seals on sterile product

Brand: Stryker Sustainability Solutions
Also listed as: BARD EP XT DECAPOLAR STEERABLE

Recalls naming this model

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,…

Company / brand: Stryker Sustainability Solutions recalls

Affected product: BARD EP XT DECAPOLAR STEERABLE recall status

Official ID Z-0085-2027 · Official record ↗

FDA Class II · Medical device · May 20, 2026

BARD EP XT Decapolar Steerable recall — Stryker Sustainability Solutions

Incomplete seals on sterile product

Company / brand: Stryker Sustainability Solutions recalls

Affected product: BARD EP XT Decapolar Steerable recall status

Official ID Z-2181-2026 · Official record ↗

See all Stryker Sustainability Solutions recalls →

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FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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