Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Prime Series Stretchers (Fifth Wheel 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
Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) 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.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report