MMP 200 Articulating Booms, Catalog Number 0682-000-604SX, Product Number 0682-001-060C. Used for operating room equipme
FDA device recall Z-1611-2011 · posted 2011-03-08 · Terminated
Recall details
- Recalling firm
- Stryker Communications Corp
- Reason for recall
- Utilization of incorrect screws resulted in inadequate thread engagement reducing the load bearing capability of the product.
- Action taken
- Stryker notified consignees verbally on January 28, 2011 and by letter dated February 11, 2011.
- Root cause
- Process control
- Status
- Terminated
- Quantity affected
- 2
- Distribution
- MA, CO
- Date initiated
- 2011-01-28
- Date posted
- 2011-03-08
- Date terminated
- 2011-03-30
- Location
- Flower Mound, TX
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