Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Power-PRO 2 Recalled by Stryker Medical Division of Stryker Corporation Due to Cot may experience unintended motion due to damaged...
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 Medical Division of Stryker Corporation directly.
Affected Products
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Quantity: 465 (403 US; 62 OUS)
Why Was This Recalled?
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Medical Division of Stryker Corporation
Stryker Medical Division of Stryker Corporation has 79 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report