Z-0304-04

Stryker brand Synergy extended stay stretcher; model 1050

Name: Z-0304-04 Stryker brand Synergy extended stay stretcher; model 1050
Creator: Stryker Medical
Published: 2003-12-30
License: https://open.fda.gov/license/

Stryker Medical / initiated 2003-12-30 / Terminated

FDA source

Stryker Medical began a recall of Stryker brand Synergy extended stay stretcher; model 1050 on 2003-12-30. The reason FDA records is "Users may be pinched in the siderail assembly when raising or lowering the siderail". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0304-04
Status: Terminated
Initiated: 2003-12-30
Posted: 2004-07-20
Terminated: 2004-04-15
Recalling firm: Stryker Medical
Product: Stryker brand Synergy extended stay stretcher; model 1050
Product code: INK Stretcher, Wheeled, Powered
Reason for recall: Users may be pinched in the siderail assembly when raising or lowering the siderail.
FDA root cause: Other
Action: Customers were sent a recall letter dated December 30, 2003. The firm will visit each facility and modify the siderail assembly.
Quantity in commerce: 107
Distribution: United States and Colombia.
Product codes and lots: All units.

Product code INK

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)