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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?

  1. 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.
  2. 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.
  3. 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.

Other products in the same recall event

The FDA groups related products into one recall event (event 28135).

Sources and updates

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