FDA Recall Terminated

Technopath Multichem S Plus Level 1 - Product Usage: Multichem S Plus (Assayed) is intended for use as an assayed quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the package insert.

Recall: Z-1362-2019 · Initiated April 9, 2019

Recall

Recall Number
Z-1362-2019
Event Number
82590
Firm
Abbott Laboratories
FEI Number
1415939
Product Code
JJY
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
April 9, 2019
Terminated
December 20, 2019
Address
100 Abbott Park Rd, Bldg Ap8b, Abbott Park, IL, 60064-3502

Description

Technopath Multichem S Plus Level 1 - Product Usage: Multichem S Plus (Assayed) is intended for use as an assayed quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the package insert.

Reason

Devices were delivered without the required dry ice.

Action

On about 04/04/2019, Abbott notified customers in Latvia of the recall. Instructions included to examine inventory for any affected devices on hand, review the letter with your Medical Director or Laboratory Management and follow your laboratory protocol regarding the need for reviewing previously reported patient results, complete and return the Customer Reply form, and notify customers if the affected devices have been forwarded to other laboratories and provide them a copy of the notification letter. If replacement material is available, customers were instructed to discontinue the use of affected devices and destroy any remaining inventory according to your laboratory procedures. If replacement material is not available, immediately order replacement material. Abbott instructed customers that they may continue to use the impacted material as long as controls are within range. Destroy impacted material once replacement material is available.

Distribution

Distribution to Latvia.

Quantity

1 unit