PlainRecalls
FDA Devices Low Class III Ongoing

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

Reported: January 25, 2023 Initiated: November 24, 2022 #Z-0958-2023

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Abbott Laboratories
Units Affected
70 cases
Distribution
US Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WV
Location
Irving, TX

Frequently Asked Questions

What product was recalled?
Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels. Recalled by Abbott Laboratories. Units affected: 70 cases.
Why was this product recalled?
Reaction vessels may contain a potential contaminant that could affect their optical performance.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 25, 2023. Severity: Low. Recall number: Z-0958-2023.