Z-0526-04

Stryker brand Firstcare Ultra Maternity bed and Stryker brand Adel Maternity bed, 220 volt, model 5012, with...

Name: Z-0526-04 Stryker brand Firstcare Ultra Maternity bed and Stryker brand Adel Maternity bed, 220 volt, model 5012, with...
Creator: Stryker Medical
Published: 2004-01-26
License: https://open.fda.gov/license/

Stryker Medical / initiated 2004-01-26 / Terminated

FDA source

Stryker Medical began a recall of Stryker brand Firstcare Ultra Maternity bed and Stryker brand Adel Maternity bed, 220 volt, model 5012, with night light on 2004-01-26. The reason FDA records is "A potential shock hazard exists if the night light is damaged". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0526-04
Status: Terminated
Initiated: 2004-01-26
Posted: 2004-02-10
Terminated: 2004-06-07
Recalling firm: Stryker Medical
Product: Stryker brand Firstcare Ultra Maternity bed and Stryker brand Adel Maternity bed, 220 volt, model 5012, with night light.
Product code: HDD Table, Obstetrical, Ac-Powered (And Accessories)
Reason for recall: A potential shock hazard exists if the night light is damaged.
FDA root cause: Other
Action: Recall letters dated January 21, 2003 were sent to each customer advising them of the firm''s plans to make a product field correction.
Quantity in commerce: 242
Distribution: Nationwide, Australia, Brazil, Canada, Chile, Hong Kong, Korea, Kuwait, Latin America, Mexico, Netherlands, Panama, Singapore, Switzerland, United Arab Emirates and United Kingdom.
Product codes and lots: All beds manufactured between January 1, 1997 and December 23, 2003.

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)