Stryker recalls 18" and 24" yellow/red color cuffs with potential detachment at welding connection, causing pressure loss. Affected units include specific serial numbers.
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
Stryker is recalling certain color cuffs that may detach at the welding connection, preventing proper pressure maintenance. This could lead to ineffective use during medical procedures.
The tourniquet cuffs can detach from the bladder at the welding connection, which means they may not maintain proper pressure during medical procedures. This could lead to ineffective blood flow control.
Medical professionals using these cuffs for tourniquet applications are most at risk. Owners of the recalled models should check their serial numbers.
Check for the model numbers: 5921-018-135 (18" red), 5921-018-235 (18" red), or 5921-024-235 (24" yellow). The serial numbers listed in the recall record indicate affected units.
Inspect the cuff for signs of detachment at the welding connection where it attaches to the bladder.
Reach out to Stryker Sustainability Solutions for specific guidance on affected units and next steps.
The affected models are Stryker Sustainability Solution Color Cuff 18" (Red) Quick Connect Dual Port Single Bladder REF 5921-018-135 and 5921-018-235, and 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235.
Check your serial numbers against the list provided in the recall record. Affected units have specific serial numbers listed for each model.
Inspect the cuff for detachment at the welding connection and contact Stryker Sustainability Solutions for further instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1804-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1804-2026 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.
