Beckman Coulter recalls certain Access 2 Reaction Vessels with possible manufacturing deformities that could cause instrument errors and delay patient results. Affected lots include P243943 through P250005.
It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities. The bottom (round end) of the Reaction Vessel may have a small protrusion or hair like deformity. This could cause causing instrument errors (e.g., pipetting, rake, wash carousel errors) that could delay patient results.
Beckman Coulter is recalling specific lots of Access 2 Reaction Vessels due to potential manufacturing deformities. These small protrusions could cause instrument errors during patient testing, potentially delaying results.
The reaction vessels may have a small protrusion or hair-like deformity at the bottom. This can cause errors in the instrument's pipetting, rake, or wash carousel functions, leading to delayed patient results.
Healthcare facilities using the Access 2 Immunoassay system with affected lots may be impacted. Laboratory staff handling these reaction vessels are most at risk of delayed patient results.
Check the lot numbers on the vessel: P243943, P243971, P244202, P244344, P244345, P250001, P250002, P250003, P250004, and P250005. These are the affected lots for the Access 2 Reaction Vessels.
Verify the lot number on the vessel to see if it matches the affected lots listed: P243943, P243971, P244202, P244344, P244345, P250001, P250002, P250003, P250004, or P250005.
The reaction vessels may have a small protrusion or hair-like deformity at the bottom that can cause instrument errors during patient testing.
Affected lots include P243943, P243971, P244202, P244344, P244345, P250001, P250002, P250003, P250004, and P250005.
No immediate stop is required; check the lot numbers to see if your vessels are affected.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-0889-2026 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-0889-2026 from Beckman Coulter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
