RecallDepth

Alinity i Processing Module, (a) Part Number 03R65-01 (b) Part Number A-30108552-01 (c) Part Number A-30109694-01 Product Usage: The Alinity i processing module is a fully automated immunoassay analyzer allowing random and continuous access, as well as priority and automated retest processing using chemiluminescent microparticle immunoassay (CMIA) technology. CMIA technology is used to determine the presence of antigens, antibodies, and analytes in samples.

This recall has been terminated (originally issued December 20, 2018).

Company
Abbott Gmbh & Co. Kg Max-Planck-Ring 2 65205 Wiesbaden Germany
Recall Initiated
December 20, 2018
Terminated
September 19, 2022
Recall Number
Z-0789-2019
Quantity
434 units
Official Source
View on FDA website ↗

Reason for Recall

Abbott has identified an issue with the Alinity i Gear Pump Assembly (part number A 30108552 01) resulting in foaming/bubbling out of the bottle reservoir for Concentrated Wash Buffer and an unexpected amount of dried residue of buffer. The foaming/bubbling is a result of an improper calibration of the pump s operating speed.

Distribution

Worldwide Distribution

Lot / Code Info

(a) Serial Numbers: Ai01001 - Ai01455, Ai01457, Ai01459 (b) all Serial Numbers (c) all Serial Numbers

Root Cause

Process control

Action Taken

The firm initiated the recall by letter on 12/20/2018. The letter identified the affected product, problem and actions to be taken. The units will be serviced in the field. For questions contact Customer Service at 1-877-4ABBOTT. Customers outside the U.S., contact your local area Customer Service.

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