Z-0023-05

Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092

Name: Z-0023-05 Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092
Creator: Stryker Medical
Published: 2004-08-17
License: https://open.fda.gov/license/

Stryker Medical / initiated 2004-08-17 / Terminated

FDA source

Stryker Medical began a recall of Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092 on 2004-08-17. The reason FDA records is "Locking pins may be installed backward, and cot may drop from highest to lowest position when the users are not prepared for the drop". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0023-05
Status: Terminated
Initiated: 2004-08-17
Posted: 2004-10-20
Terminated: 2004-10-19
Recalling firm: Stryker Medical
Product: Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.
Product code: FPO Stretcher, Wheeled
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.
FDA root cause: Other
Action: Service representatives visited each customer, inspected the cots, and reinstalled the lock pins, if required, beginning on August 10, 2004.
Quantity in commerce: 15
Distribution: Alabama, California, Florida, Kansas, Montana, Oklahoma, Texas and Virginia.
Product codes and lots: Serial numbers 040639739, 040639849, 040639737, 040639738, 040639675, 040639674, 040639670, 040639671, 040639672, 040639716, 040639847, 040639848, 040639935, 040639936 and 040639937.

Product code FPO

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)