Timberline Cranial Caudal and Posterior Blades, 40 - 180mm Model # 8734-2XXX, 8734-5XXX is a reusable device provided wi
FDA device recall Z-1069-2015 · posted 2015-02-09 · Terminated
Recall details
- Recalling firm
- Biomet Spine, LLC
- Reason for recall
- Biomet Spine, LLC is recalling the Timberline Cranial Caudal and Posterior Blades, 40-180mm due to oversize of the set screw hex feature.
- Action taken
- Biomet initiated the recall on February 22, 2012, No letters were or will be sent to customers. 100% retrieval was achieved by working directly with the customers. For questions regarding this recall call 303-501-8548.
- Root cause
- Nonconforming Material/Component
- Status
- Terminated
- Product code
- MAX
- Quantity affected
- 213
- Distribution
- Distributed to TX, IN, MO, and NY. No foreign/govt/military/VA.
- Date initiated
- 2012-02-22
- Date posted
- 2015-02-09
- Date terminated
- 2015-03-23
- Location
- Broomfield, CO
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