FDA Medical Device Recalls (openFDA)
Stryker Medical: Stryker brand Firstcare Ultra Maternity bed, model 5010, with night light.
- Recall number
- Z-0525-04
- Recalling firm
- Stryker Medical
- Product
- Stryker brand Firstcare Ultra Maternity bed, model 5010, with night light.
- Status
- Terminated
- Initiated
- 2004-01-26
- Posted
- 2004-02-10
- Terminated
- 2004-06-07
- Reason
- A potential shock hazard exists if the night light is damaged.
- 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
- 763
- Distribution
- Nationwide, Australia, Brazil, Canada, Chile, Hong Kong, Korea, Kuwait, Latin America, Mexico, Netherlands, Panama, Singapore, Switzerland, United Arab Emirates and United Kingdom.
- Lot, serial or model codes
- All beds manufactured between January 1, 1997 and December 23, 2003.
- 510(k) numbers
- ["K950889"]
- PMA numbers
- not on file
- Product code
- HDD
- Firm FEI
- 1831750
- Firm city
- Kalamazoo
- Firm state
- MI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28