Stryker brand Adel maternity bed, model 4700, with night… recallZ-0524-04 · Stryker Medical · initiated Jan 26, 2004
Terminated All recalls posted in February 2004
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Stryker Medical or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
A potential shock hazard exists if the night light is damaged.
FDA root cause category: Other
What the company is doing
Recall letters dated January 21, 2003 were sent to each customer advising them of the firm''s plans to make a product field correction.
Recall details
- Recall number
- Z-0524-04
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Jan 26, 2004
- Posted by the FDA
- Feb 10, 2004
- Recalling firm
- Stryker Medical
- Quantity
- 1391
- Product code
- HDD
- FDA submissions
- K950889
- Distribution
- Nationwide, Australia, Brazil, Canada, Chile, Hong Kong, Korea, Kuwait, Latin America, Mexico, Netherlands, Panama, Singapore, Switzerland, United Arab Emirates and United Kingdom.
Product description
Stryker brand Adel maternity bed, model 4700, with night light.
Code information (models, lots, serial numbers)
All beds manufactured between August 1, 2000 and December 23, 2003.
Other devices under the same FDA submission
1 device cleared under K950889 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- NA 4701Stryker Corporation · TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES)129 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 28135).
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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