Randox recalls Assayed Bovine Multi-Sera Level 1 Model AL1027 Lot 205SL due to potential bile acids measurement errors. Affected users should contact Randox for details.
The firm is re-assigning the Mean of all Instruments target and range for Bile Acids (5th Generation Colorimetric) in the Assayed Bovine Multi-Sera Level 1 Control Lot 205SL.
Randox is recalling a specific lab test kit (Assayed Bovine Multi-Sera Level 1, Model AL1027) because of a problem with how it measures bile acids. This could lead to inaccurate test results if used improperly.
The kit has a calibration issue with the bile acids measurement target. This could cause incorrect test results if the kit is used without proper adjustments. The problem affects only specific lab test results, not the physical safety of the device.
Lab users who purchased the Assayed Bovine Multi-Sera Level 1, Model AL1027, Lot 205SL from Randox. Those performing bile acid tests with this kit are most at risk of inaccurate results.
Check for the model number AL1027 and lot number 205SL on the product label. This recall applies to the Assayed Bovine Multi-Sera Level 1 test kit used for bile acid measurements.
Verify the model number AL1027 and lot number 205SL on the product label.
The recall is due to a calibration issue with bile acids measurement in the Assayed Bovine Multi-Sera Level 1 test kit, which could lead to inaccurate test results.
The recall record does not specify a remedy, so contact Randox directly for further instructions.
The recall indicates a potential for inaccurate test results, not physical harm. This is considered a low-risk issue.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-2207-2019 — Randox Randox Hello, I own a Randox that is covered by recall Z-2207-2019 from Randox. 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.
