Medical Device Recall: Z-0026-04

FDA Recalls dataset · Firm: Surgical Specialties Corp · Status: Terminated

Recall Action Class: N/A Date Initiated: 2003-08-21 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0026-04.

Recall Res Number
Z-0026-04
Recalling Firm / Manufacturer
Surgical Specialties Corp
FEI Number
2522801
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2003-08-21
Date Posted
2003-10-15
Date Terminated
2004-01-13
Product Code
HNN
Event Number
27154
Product Quantity
666 units
Product Description Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
Reason for Recall text on product handle is incorrect
Action Details The consignees were notified via fax on 8/21/03. One customer received a recall letter via mail on 8/22/03.
Distribution Pattern The products were shipped to two hospitals in CA, two sales representatives in NC & IL, and three wholesalers in IL, Belgium, Canada, and Austrailia.
Code Information / Serial Numbers M190500 exp 11/2007 and M203840 exp 12/2007

Related Establishments / Registrations

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This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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