Medical Device Recall: Z-0022-2009

FDA Recalls dataset · Firm: Becton Dickinson and Company · Status: Terminated

Recall Action Class: N/A Date Initiated: 2008-09-15 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0022-2009.

Recall Res Number
Z-0022-2009
Recalling Firm / Manufacturer
Becton Dickinson and Company
FEI Number
1211998
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2008-09-15
Date Posted
2008-10-03
Date Terminated
2012-02-29
Product Code
HMX
Event Number
49436
Product Quantity
1485 units
Product Description BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for Vitroretinal Surgery.
Reason for Recall Product labeled as 4 mm High Viscosity Injector tip contains a 6 mm tip.
Action Details BD contacted accounts by telephone on 9/15/08 requesting users to discard units and complete the response form. Contact Becton Dickinson and Co. at 1-781-906-7950 for assistance.
Distribution Pattern AZ, CA, CO, IL, OH, FL, PA , TN, TX,and VA Foreign: Australia and Japan.
Code Information / Serial Numbers Lot Number: 8018591

Related Establishments / Registrations

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