FDA Recall
Terminated
Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)
Recall: Z-0530-05
·
Initiated January 14, 2005
Recall
- Recall Number
- Z-0530-05
- Event Number
- 30997
- Firm
- Interpore Cross International Inc
- FEI Number
- 1000160576
- Product Code
- MQP
- Status
- Terminated
- Root Cause
- Other
- Initiated
- January 14, 2005
- Posted
- February 4, 2005
- Terminated
- March 3, 2005
- Address
- 181 Technology Dr, Irvine, CA, 92618-2402
Description
Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)
Reason
Mislabeled.
Action
Firm sent recall letters on 1/18/2005 requesting return of product. A response form was enclosed.
Distribution
TN, MT, MI, CA, IN, PA, NJ, TX, KY, LA, CO.
Quantity
63