Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zimmer Tourniquet Cuff 30" (Blue) Recalled by Stryker Sustainability Solutions Due to Mislabeling
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Sustainability Solutions directly.
Affected Products
Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868, Reprocessed Tourniquet Cuff - Product Usage: Reprocessed tourniquet cuffs are indicated for use in patients who require surgery of the extremities with an expected duration of less than 90 minutes when temporary exsanguination of a limb is desired.
Quantity: 90
Why Was This Recalled?
Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadequate Limb Compression Force.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Sustainability Solutions
Stryker Sustainability Solutions has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report