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