Recall Z-2353-2016— Stryker Medical Division of Stryker Corporation
Class II · Terminated
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2016-02-02, terminated 2017-06-12. FDA's recall record names no specific 510(k) clearance for this event. Product: S3 MedSurg Bed, Model 3005. Stryker Medical. Reason: CPU board failures cause fowler (backrest) electronic controls to stop working..
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-02-02
- Terminated
- 2017-06-12
- Firm location
- Portage, MI, United States
Product description
S3 MedSurg Bed, Model 3005. Stryker Medical
Reason for recall
CPU board failures cause fowler (backrest) electronic controls to stop working.
Data sourced from openFDA. This site is unofficial and independent of the FDA.