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Terminated

Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)

FDA Recall Z-0530-05 · Posted 2005-02-04

Recalling FirmInterpore Cross International Inc
Recall StatusTerminated
Product CodeMQP
Date Initiated2005-01-14
Date Terminated2005-03-03
Product Quantity63

Reason for Recall

Mislabeled.

Firm Action

Firm sent recall letters on 1/18/2005 requesting return of product. A response form was enclosed.

Root Cause

Other

Distribution Pattern

TN, MT, MI, CA, IN, PA, NJ, TX, KY, LA, CO.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K040168MODIFICATION TO GEO STRUCTUREInterpore Cross Intl. · 2004-04-08

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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