Medtronic Sofamor Danek brand LT CAGE lumbar tapered fusion device implant 14 mm x 17.5 mm x 23 mm; Catalog number 89414
FDA device recall Z-1090-05 · posted 2005-08-06 · Terminated
Recall details
- Recalling firm
- Warsaw Orthopedic, Inc.
- Reason for recall
- The product is labeled as sterile, but this lot was not sterilized.
- Root cause
- Other
- Status
- Terminated
- Product code
- MAX
- Quantity affected
- 140
- Distribution
- United States and Canada.
- Date initiated
- 2005-05-27
- Date posted
- 2005-08-06
- Date terminated
- 2005-09-20
- Location
- Warsaw, IN
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