The FL23SE Bed is an AC-powered adjustable hospital bed with four… — Class II medical device recall Z-2283-2013
Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2013-10-02, distributed in MI, VA, WI. The nurse call cable (Part Number: QDF23-0571) on the FL23SE Bed is located right under the opening of the bed
| Recall number | Z-2283-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2013-08-19 |
| Classified | 2013-09-26 |
| Reported by FDA | 2013-10-02 |
| Terminated | 2014-01-29 |
| Distributed | MI, VA, WI |
| Countries outside the US | CA |
| Quantity | 61 units |
| Model numbers | FL23SE |
Product
The FL23SE Bed is an AC-powered adjustable hospital bed with four built-in electric DC motors and remote controls that is intended for medical purposes. It can be operated by the patient or the caregiver to adjust the height and surface contour of the bed. The bed includes movable and latchable siderails. The FL23SE Bed is intended for use with patients for procedures, therapy, recovery in healthcare environments, and to transport patients between bays and procedural rooms. The FL23SE Bed is intended for use with patients for procedures, therapy, recovery in healthcare environments, and to transport patients between bays and procedural rooms.
Reason for recall
The nurse call cable (Part Number: QDF23-0571) on the FL23SE Bed is located right under the opening of the bed head box. If an accessory (i.e. IV pole) is inserted into this slot, the circuit directing the nurse call system can be damaged.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.