Stryker Visum 300 Ceiling-mounted Exam Light.
FDA device recall Z-1992-2013 · posted 2013-08-21 · Terminated
Recall details
- Recalling firm
- Stryker Communications
- Reason for recall
- Potential incomplete final weld on the drop tube flange.
- Action taken
- The firm decided to recall and notified consignees with an "Urgent Medical Device Correction/Removal" notification letter dated 07/29/13. The product issue was described and recommended actions were provided. Customers may contact Stryker Technical Support at 866-841-5663.
- Root cause
- Process control
- Status
- Terminated
- Product code
- KZF
- Quantity affected
- 1,375 units
- Distribution
- Worldwide Distribution: US natiowide and to the country of Canada.
- Date initiated
- 2013-07-25
- Date posted
- 2013-08-21
- Date terminated
- 2015-04-03
- Location
- Flower Mound, TX
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