Medical Device Recall: Z-0013-05

FDA Recalls dataset · Firm: Biomet, Inc. · Status: Terminated

Recall Action Class: N/A Date Initiated: 2004-07-07 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0013-05.

Recall Res Number
Z-0013-05
Recalling Firm / Manufacturer
Biomet, Inc.
FEI Number
1825034
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2004-07-07
Date Posted
2004-10-08
Date Terminated
2004-10-07
Product Code
HTY
Event Number
29513
Product Quantity
37
Product Description Lactosorb pin, 2.0 x 20 mm, sterile; ref. 948205.
Reason for Recall Mislabeled as to size; 1.55 mm pins are labeled as 2mm.
Action Details Consignees were notified by recall letter dated July 7, 2004 and sent via fax.
Distribution Pattern Colorado, Mississippi, Missouri, Montana, New York, Ohio, Pennsylvania, Texas and Wisconsin.
Code Information / Serial Numbers Lot 439010 Exp. 2006-11.

Related Establishments / Registrations

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