Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Transport Stretcher Recalled by Stryker Medical Division of Stryker Corporation Due to The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...
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
Transport Stretcher, and Head and Neck Surgery Stretcher Non-powered stretcher
Quantity: 36
Why Was This Recalled?
The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) were manufactured using the incorrect oil. The oil used does not contain the same wear resistance additives as the specified oils and therefore its use increases the potential for wear which may cause a leak event or jack drift. Testing was done to evaluate the jacks with incorrect oil and leak events we
Where Was This Sold?
This product was distributed to 15 states: AL, CA, FL, MN, MT, NE, NY, NC, PA, RI, TN, TX, UT, WV, DC
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