Stryker recalls BARD Dynamic Tip Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall notice.
Incomplete seals on sterile product
Stryker is recalling BARD Dynamic Tip Steerable catheters that have incomplete sterile seals. This could lead to contamination during medical procedures if the catheter is used improperly.
Incomplete seals on the catheter could allow contamination during medical procedures. This might lead to infections or other complications if the catheter is not properly sterilized.
Healthcare professionals using the catheter for electrophysiology procedures are most at risk. Patients receiving these catheters during medical treatments may be affected if the seal is compromised.
Check for the product number 200131 and lot numbers listed in the recall notice. The catheter has a unique device identifier (UDI) starting with 00885825002930.
Verify the product number and lot numbers listed in the recall notice to confirm if your catheter is affected.
The recall indicates incomplete sterile seals, which could compromise safety during medical procedures. Affected units should not be used until the recall is addressed.
Check the product number and lot numbers listed in the recall notice to determine if your catheter is affected. If it is, contact Stryker for further instructions.
Look for the product number 200131 and lot numbers from the list provided in the recall notice. The catheter also has a unique device identifier (UDI) starting with 00885825002930.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2175-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2175-2026 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
