FDAClass IIIJanuary 25, 2023

Alinity Reaction Vessels recall

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

Why was Alinity Reaction Vessels recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI/Lots: 00380740129026/000586790 and 000586879

Product
Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels
Recalling firm
Abbott Laboratories
Quantity
70 cases
Distribution
US Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WV
Recall date
January 25, 2023
Classification
Class III
Status
Ongoing
Agency
FDA (device)
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