Stryker recalls expired sterile surgical cannulas for potential use in procedures. Affected items have specific catalog and lot numbers. Consumers should contact Stryker for details.
Expired Products distributed to customers
Stryker is recalling expired sterile surgical cannulas that could be unsafe for medical procedures. Using expired products may lead to improper use or complications during surgery.
Expired products may not function properly during surgery, potentially leading to incorrect placement of the lesion. This could cause complications or injuries during medical procedures.
Medical professionals who use these cannulas for surgical procedures. Patients undergoing surgery with expired cannulas may face risks.
Check for catalog number 0406-630-225 and lot number 1000388946 on the product packaging. These items were distributed to customers starting from the date of manufacture.
Look for catalog number 0406-630-225 and lot number 1000388946 on the product packaging.
The products are expired and may not function properly during surgery, potentially causing complications.
Check for catalog number 0406-630-225 and lot number 1000388946 on the product packaging.
Contact Stryker Corporation for further instructions on how to handle the product.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2261-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2261-2024 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.
