Z-0554-06

Stryker Epic Critical Care Bed; Model 2030

Name: Z-0554-06 Stryker Epic Critical Care Bed; Model 2030
Creator: Stryker Medical
Published: 2006-01-17
License: https://open.fda.gov/license/

Stryker Medical / initiated 2006-01-17 / Terminated

FDA source

Stryker Medical began a recall of Stryker Epic Critical Care Bed; Model 2030 on 2006-01-17. The reason FDA records is "The bed exit may not alarm as appropriate". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0554-06
Status: Terminated
Initiated: 2006-01-17
Posted: 2006-03-31
Terminated: 2006-07-03
Recalling firm: Stryker Medical
Product: Stryker Epic Critical Care Bed; Model 2030.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: The bed exit may not alarm as appropriate.
FDA root cause: Other
Action: The firm began visiting accounts to install new software on 1/17/06 and expects completion of installation at all accounts by 3/31/06.
Quantity in commerce: 68
Distribution: World Wide--(Chile, Mexico and Singapore)
Product codes and lots: Serial numbers 0512068638, 0512068639, 0512068640, 0512068641, 0512068642, 0512068667, 0512068668, 0512068669, 0512068670, 0512068725, 0512068726, 0512068727, 0512068728, 0512068740, 0512068750, 0512068751, 0409060679, 0409060680, 0409060681, 0409060682, 0409060683, 0409060684, 0409060685, 0409060686, 0409060687, 0512068643, 0512068644, 0512068645, 0512068646, 0512068647, 0512068648, 0512068649, 0512068650, 0512068651, 0512068652, 0512068653, 0512068654, 0512068655, 0512068656, 0512068657, 0512068658, 0512068659, 0512068660, 0512068661, 0512068662, 0512068779, 0512068780, 0512068781, 0512068782, 0512068783, 0512068784, 0512068785, 0512068709, 0512068710, 0512068711, 0512068712, 0512068713, 0512068714, 0512068715, 0512068716, 0512068717, 0512068718, 0512068719, 0512068720, 0512068721, 0512068722, 0512068723 and 0512068724.

Product code FNL

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)