Stryker recalls CS Uni-Directional w Auto ID catheters with Product Number D135303 due to incomplete sterile seals. Affected units include specific lot numbers. Stop using immediately to prevent infection risks.
Incomplete seals on sterile product
Stryker is recalling CS Uni-Directional w Auto ID electrocardiography catheters (Product Number D135303) because they have incomplete sterile seals. This could lead to infections if used in medical procedures.
Incomplete seals on the sterile product can allow contaminants to enter the catheter during use. This increases the risk of infection for patients during medical procedures.
Healthcare professionals and medical facilities that use this catheter for electrophysiology procedures. Patients undergoing these procedures are at risk of infection if the recalled catheter is used.
Look for the Product Number D135303 and Lot Numbers listed in the recall notice (e.g., 2934107, 3695884, 3813841, etc.). The catheter has a UDI (Unique Device Identifier) of 07613327357301.
Discontinue use of the recalled catheter to prevent potential infection risks.
The product number is D135303.
Affected lot numbers include 2934107, 3695884, 3813841, and others listed in the recall notice.
Check the Product Number D135303 and Lot Numbers listed in the recall notice (e.g., 2934107, 3695884, etc.).
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2184-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2184-2026 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.
