Recall Z-1185-2017— Invacare Corporation
Class II · Terminated
Class II FDA medical device recall by Invacare Corporation, initiated 2016-12-02, terminated 2017-11-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Junction Box - 1104343 and 1193560. Reason: A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire..
- Recalling firm
- Invacare Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-12-02
- Terminated
- 2017-11-02
- Firm location
- Elyria, OH, United States
Product description
Junction Box - 1104343 and 1193560
Reason for recall
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
Data sourced from openFDA. This site is unofficial and independent of the FDA.