FDA Recall Terminated

Clinical Chemistry Alkaline Phosphatase, List Number 7D55-21 & 7D55-31. Used for the quantitation of alkaline phosphatase in human serum or plasma.

Recall: Z-3278-2011 · Initiated August 26, 2011

Recall

Recall Number
Z-3278-2011
Event Number
59862
Firm
Abbott Laboratories, Inc
FEI Number
1628664
Product Code
CJE
Status
Terminated
Root Cause
Pending
Initiated
August 26, 2011
Posted
September 26, 2011
Terminated
August 17, 2012
Address
1921 Hurd Drive PO Box 152020, Irving, TX, 75038-4313

Description

Clinical Chemistry Alkaline Phosphatase, List Number 7D55-21 & 7D55-31. Used for the quantitation of alkaline phosphatase in human serum or plasma.

Reason

The reagent has the potential to be contaminated with mold, the Cladosporium fungal species.

Action

The firm decided to recall and notified consignees by a Product Recall - Immediate Action Required letter on 08/26/11. The letter identified the affected product, the reason for the recall, the patient impact, and necessary actions to be taken by the customer. Customers are to determine if they are using or have the affected product in their inventory. Customers are to discontinue use and destroy any remaining product of the specified lots in accordance with their facility's policies and procedures. Alternative lots of the product should be ordered and the enclosed Customer Reply form should be completed and returned. The letter also states that customers may want to decontaminate their systems by following the steps in Attachment A. If the product from the affected lots were further distributed, a copy of the letter should be provided to those customers as well. Questions regarding the letter should be directed to Customer Service at 1-877-4ABBOTT for US customers, and customers outside of the US should contact their local area Customer Service.

Distribution

Worldwide Distribution

Quantity

6269 units