Recall Z-1992-2013— Stryker Communications
Class II · Terminated
Class II FDA medical device recall by Stryker Communications, initiated 2013-07-25, terminated 2015-04-03. FDA's recall record names no specific 510(k) clearance for this event. Product: Stryker Visum 300 Ceiling-mounted Exam Light.. Reason: Potential incomplete final weld on the drop tube flange..
- Recalling firm
- Stryker Communications
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-07-25
- Terminated
- 2015-04-03
- Firm location
- Flower Mound, TX, United States
Product description
Stryker Visum 300 Ceiling-mounted Exam Light.
Reason for recall
Potential incomplete final weld on the drop tube flange.
Data sourced from openFDA. This site is unofficial and independent of the FDA.