Recall Z-1555-2016— Stryker Medical Division of Stryker Corporation
Class II · Terminated
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2015-07-02, terminated 2017-03-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Spirit One A-C Powered Hospital Bed. Reason: Customer complaints associated with faulty brake system.
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-07-02
- Terminated
- 2017-03-24
- Firm location
- Portage, MI, United States
Product description
Spirit One A-C Powered Hospital Bed
Reason for recall
Customer complaints associated with faulty brake system
Data sourced from openFDA. This site is unofficial and independent of the FDA.