Stryker recalls blue 30" Zimmer tourniquet cuffs with potential mislabeling that could cause improper use or inadequate limb compression during procedures.
Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadequate Limb Compression Force.
Stryker is recalling blue 30-inch Zimmer tourniquet cuffs that may be mislabeled. This could lead to improper use or insufficient limb compression during medical procedures, risking patient safety.
Mislabeling could cause the tourniquet to be used incorrectly or not provide enough pressure to compress the limb properly. This might lead to improper blood flow during surgical procedures.
Healthcare professionals using these specific tourniquet cuffs for extremity procedures are most at risk. Patients undergoing surgery with these cuffs may experience inadequate limb compression.
Check for the blue color, 30-inch size, PLC Dual Port, Single Bladder, and item number 60-7070-105. The unique device identifier (UDI) 00885825013868 also identifies this specific model.
Look for the blue color, 30-inch size, PLC Dual Port, Single Bladder, and item number 60-7070-105 on the cuff.
The tourniquet cuffs may be mislabeled, which could lead to improper use or inadequate limb compression during procedures.
The recall record does not specify a remedy, so check the product label to confirm if it matches the recalled model.
The recall indicates potential mislabeling that could cause improper use or inadequate compression, so it's recommended to verify the label before use.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1802-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1802-2020 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.
