Medical Device Recall: Z-0023-05

FDA Recalls dataset · Firm: Stryker Medical · Status: Terminated

Recall Action Class: N/A Date Initiated: 2004-08-17 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0023-05.

Recall Res Number
Z-0023-05
Recalling Firm / Manufacturer
Stryker Medical
FEI Number
1831750
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2004-08-17
Date Posted
2004-10-20
Date Terminated
2004-10-19
Product Code
FPO
Event Number
29864
Product Quantity
15
Product Description Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.
Reason for Recall Locking pins may be installed backward, and cot may drop from highest to lowest position when the users are not prepared for the drop.
Action Details Service representatives visited each customer, inspected the cots, and reinstalled the lock pins, if required, beginning on August 10, 2004.
Distribution Pattern Alabama, California, Florida, Kansas, Montana, Oklahoma, Texas and Virginia.
Code Information / Serial Numbers Serial numbers 040639739, 040639849, 040639737, 040639738, 040639675, 040639674, 040639670, 040639671, 040639672, 040639716, 040639847, 040639848, 040639935, 040639936 and 040639937.

Related Establishments / Registrations

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This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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