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Terminated

Stryker Medical -Wheeled Electric Stretcher, Model 1550 (with and without scales)

FDA Recall Z-1009-2007 · Posted 2007-09-21

Recalling FirmStryker Medical Div. of Stryker Corporation
Recall StatusTerminated
Product CodeFPO
Date Initiated2007-05-07
Date Terminated2008-06-11
Product Quantity1,048 (1009 in the U.S. plus 39 international)

Reason for Recall

The internal power cord may become damaged due to wear and, if this occurs, a shock hazard exists.

Firm Action

Consignees were notified of the problem via letter dated 5/7/07 instructing them to immediately unplug the affected stretchers with scales, affix a warning label enclosed with the letter to the power cord of stretchers with scales, and that they will be contacted so that the firm can schedule a visit to upgrade all affected stretchers. A second notification letter was issued on August 7, 2007 to cover all 1550 stretchers with and without scales.

Root Cause

Other

Distribution Pattern

Worldwide: USA, Latin America, Mexico and Spain.

Official Source

View FDA Recall →

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

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