Stryker recalls disposable tourniquet cuffs that may not hold pressure properly, risking blood loss during surgery. Affected units have specific catalog numbers and lot dates. Consumers should contact Stryker for details.
Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, may lead to operative site blood loss, hemorrhage or, in exceedingly rare situations, other major complications
Stryker is recalling disposable tourniquet cuffs that may not hold pressure correctly during use, potentially causing blood loss or bleeding during surgery. This recall affects specific model numbers and production lots.
The cuffs may not achieve or maintain the required pressure when first applied to a patient, which could lead to blood loss at the surgical site. In rare cases, this might cause serious complications during surgery.
Surgical staff and patients using the recalled tourniquet cuffs during procedures. Those with the specific catalog number and lot dates are most at risk.
Check for the catalog number 5921-034-135NS and lot numbers from 2022111805 to 2022120508 on the product packaging. The product is sold as a disposable tourniquet cuff for surgical use.
Look for the catalog number 5921-034-135NS and lot numbers from 2022111805 to 2022120508 on the product packaging.
The cuffs may not hold pressure properly when first applied, potentially causing blood loss or bleeding during surgery.
Check for the catalog number 5921-034-135NS and lot numbers from 2022111805 to 2022120508 on the product packaging.
Contact Stryker directly for instructions on how to handle the product, as the recall remedy is not specified in the record.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1341-2023 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1341-2023 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.
