RecallDepth

Variant II Turbo Hemoglobin A1c Program, model number 270 2417, manufactured by Bio-Rad Laboratories, Inc, Hercules, CA. Intended Use: For the percent determination of hemoglobin A1c in human whole blood using ion-exchange high-performance liquid chromatography (HPLC).

Company
Bio-Rad Laboratories Inc
Recall Initiated
October 12, 2009
Posted
February 26, 2010
Terminated
December 17, 2010
Recall Number
Z-0867-2010
Quantity
21 kits
Firm Location
Hercules, CA

Reason for Recall

Product update kit CD rom will not upload. As a result, the device cannot be run.

Distribution

Worldwide Distribution -- USA, Hong Kong, and New Zealand.

Lot / Code Info

Lot No. 70291520.

Root Cause

Other

Action Taken

The firm initiated this action on 10/12/2009. Consignees were contacted by phone with a fax follow up. Subsidiaries, as well as consignees that received the product, were provided with a Medical Device Correction notice, dated October 13, 2009, and response form. Each subsidiary will contact customers. The letter asks customers to destroy the affected lot included with their reorder packs and replace them with the lot number that's enclosed. Customers are to complete the Customer Medical Device Correction Response Form and fax it to Bio-Rad CSD Regulatory Affairs Department at the number provided. Questions should be directed to customers' regional Bio-Rad office.

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