FDAFebruary 7, 2024device

Access Substrate, REF 81906, For use with the Access Immunoassay Systems

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

On 07 February 2024 Beckman Coulter made the decision to conduct a field action on Access Substrate (81906) lots: 234600, 337984, 338040, 338214, 338229, 338289, 338322, 338333, 338451, 338587, and 338538. Beckman Coulter has identified that Access Substrate bottles in the identified lots were released from manufacturing without labels. Missing label may cause some patient results reporting delay but will not cause any errorreous results. However, because labs are required to have redundancy such that delay would not significantly impact clinical management and because the defect is easily recognized by the user, the probability of harm is remote.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

15099590229986

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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