Beckman Coulter recalls MicroScan autoSCAN-4 Instruments with incorrect diffuser plates. Affected units have specific serial numbers; contact for replacement.
Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect diffuser plate.
Beckman Coulter is recalling MicroScan autoSCAN-4 Instruments that were manufactured with an incorrect diffuser plate. This issue could lead to improper function of the instrument, though serious injury risks are not specified in the recall notice.
The instrument uses a diffuser plate to direct light for testing. An incorrect plate may cause improper light distribution, leading to inaccurate test results. However, the recall does not mention physical harm or injury risks.
Lab users who own or use MicroScan autoSCAN-4 Instruments with the specific serial numbers listed in the recall. Those with the incorrect diffuser plate are most at risk.
Check if your MicroScan autoSCAN-4 Instrument has the serial numbers listed in the recall (e.g., 400495-400524, 400528). Also, verify the diffuser plate part number P/N 5639-0001.
Compare your instrument's serial number with the list of affected units provided in the recall notice.
Reach out to Beckman Coulter for instructions on replacement or repair if your unit is affected.
The instrument was manufactured with an incorrect diffuser plate, which may cause improper light distribution during testing.
Check if your serial number matches the list of affected units (e.g., 400495-400524, 400528) or if your diffuser plate has part number P/N 5639-0001.
The recall does not specify a risk of serious injury, so no immediate stop is required. However, affected units should be checked for replacement.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-0269-2023 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-0269-2023 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.
