Z-0793-05

Stryker brand Birthing Bed; Model 4701

Name: Z-0793-05 Stryker brand Birthing Bed; Model 4701
Creator: Stryker Medical
Published: 2005-03-31
License: https://open.fda.gov/license/

Stryker Medical / initiated 2005-03-31 / Terminated

FDA source

Stryker Medical began a recall of Stryker brand Birthing Bed; Model 4701 on 2005-03-31. The reason FDA records is "Trendelenburg and reverse trendelenburg features may not function". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0793-05
Status: Terminated
Initiated: 2005-03-31
Posted: 2005-05-03
Terminated: 2005-05-09
Recalling firm: Stryker Medical
Product: Stryker brand Birthing Bed; Model 4701.
Product code: HDD Table, Obstetrical, Ac-Powered (And Accessories)
Reason for recall: Trendelenburg and reverse trendelenburg features may not function.
FDA root cause: Other
Action: Consignees were notified via letter dated 3/31/05 and Stryker personnel began visiting the facilities to make corrections.
Quantity in commerce: 31
Distribution: California, Georgia, Indiana, Iowa, Michigan, Ohio and Pennsylvania.
Product codes and lots: All units manufactured 10/18 through 11/05/04.

Product code HDD

K950889Class IIAdel 5000Stryker Corp. / cleared 1995-10-16

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)