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Terminated

Stryker Power-PRO Powered Ambulance Cot, Model 6500.

FDA Recall Z-1513-06 · Posted 2006-09-22

Recalling FirmStryker Medical Div. of Stryker Corporation
Recall StatusTerminated
Product CodeFPO
Date Initiated2006-08-29
Date Terminated2007-04-18
Product Quantity1,841 cots (44 foreign)

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.

Firm Action

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

Distribution Pattern

Worldwide distribution ---- including USA and countries of Canada, China, Germany and Switzerland.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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