Beckman Coulter recalls MicroScan PROMPT Inoculation System-D with incorrect wands that may cause false test results. Affected units have catalog number B1026-10D and UDI 15099590659561. Contact for remedy.
Due to customer reports it has been determined that the inoculation system contains the incorrect prompt wands. Use of the incorrect wands could result in false -susceptible results, false-resistant results, possible misidentifications, or possible out-of-range Quality Control results.
Beckman Coulter is recalling a specific inoculation system used in lab testing because it contains the wrong wands. Using these incorrect wands can lead to false results in antimicrobial susceptibility tests, which might cause misidentifications or incorrect treatment decisions.
The inoculation system contains incorrect wands that can produce false results. This means tests might show bacteria as susceptible when they're resistant, or vice versa. It could lead to wrong treatment decisions if the lab relies on these results.
Lab technicians and healthcare professionals who use this specific inoculation system for antimicrobial testing. Those handling the recalled units with catalog number B1026-10D are most at risk.
Check for catalog number B1026-10D and unique device identifier (UDI) 15099590659561. The product was sold with lot number 20201103T and expired November 3, 2020.
Verify the catalog number and UDI to confirm if your unit is affected.
Using the incorrect wands could result in false susceptible results, false resistant results, possible misidentifications, or out-of-range Quality Control results.
Check for catalog number B1026-10D and unique device identifier (UDI) 15099590659561.
The recall record does not specify a remedy.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1674-2020 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1674-2020 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.
