Stryker Medical Div. of Stryker Corporation Stryker Power-PRO Powered Ambulance Cot, Model 6500. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Power-PRO Powered Ambulance Cot, Model 6500.
Brand
Stryker Medical Div. of Stryker Corporation
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
All units with a serial number lower than 060739380. (units manufactured between 1 Oct 2005 and 15 July 2006)
Stryker Medical Div. of Stryker Corporation is recalling Stryker Power-PRO Powered Ambulance Cot, Model 6500. due to The head section wheel assembly may flex outward from the cot because the head section wheel bolts, which hold the assembly upright, may back out.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The head section wheel assembly may flex outward from the cot because the head section wheel bolts, which hold the assembly upright, may back out.
Recommended Action
Per FDA guidance
Consignees were notified of the recall via letter dated 8/29/06. Included with the letter were replacement bolts for each cot and installation instructions, but the customer was given the option of contacting the recalling firm for installation.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026