FDA Recall Open, Classified

Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels

Recall: Z-0958-2023 · Initiated November 24, 2022

Recall

Recall Number
Z-0958-2023
Event Number
91303
Firm
Abbott Laboratories
FEI Number
3016438761
Product Code
DHA
Status
Open, Classified
Root Cause
Material/Component Contamination
Initiated
November 24, 2022
Posted
January 17, 2023
Address
1915 Hurd Dr, Irving, TX, 75038

Description

Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels

Reason

Reaction vessels may contain a potential contaminant that could affect their optical performance.

Action

On 11/24/22, the recalling firm phoned customers and informed them of the recall using a phone script. On the same day, the phone call was followed by an email that restated the information in the phone script and included a Customer Reply form. Customers were asked to discontinue use and destroy the impacted inventory according to their laboratory procedures. If customers forwarded the product to other laboratories, they were asked to inform them of this Product Recall and complete and return the Customer Reply form, which can be returned to [email protected]. The reply form asked customers to record the number of boxes destroyed. If you have any questions, contact QA Manager, Post Market Surveillance at 224-668-0343 or email: [email protected].

Distribution

US Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WV

Quantity

70 cases