Stryker Power-PRO Powered Ambulance Cot, Model 6500.
FDA device recall Z-1513-06 · posted 2006-09-22 · Terminated
Recall details
- Recalling firm
- Stryker Medical Div. of Stryker Corporation
- Reason for recall
- 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.
- Action taken
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- FPO
- Quantity affected
- 1,841 cots (44 foreign)
- Distribution
- Worldwide distribution ---- including USA and countries of Canada, China, Germany and Switzerland.
- Date initiated
- 2006-08-29
- Date posted
- 2006-09-22
- Date terminated
- 2007-04-18
- Location
- Portage, MI
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