Fujifilm recalls Wako HDL-C/LDL-C Calibrator (Lot EL62:9) due to incorrect concentration values on labels, which may lead to inaccurate cholesterol test results. Affected units should be checked for the specific lot number.
FUJIFILM has become aware that incorrect concentration values were printed on the bottle label for all product manufactured as part of Lot EL629. This may result incorrect results when used in testing.
Fujifilm is recalling Wako HDL-C/LDL-C Calibrators from Lot EL629 because the label shows incorrect concentration values. This could cause inaccurate cholesterol test results if used in medical testing.
The calibrator's label has incorrect concentration values for the test. This could lead to inaccurate cholesterol measurements when used in medical testing, potentially affecting health decisions.
People who own or use the Wako HDL-C/LDL-C Calibrator with Lot EL629 for cholesterol testing are affected. Those who rely on accurate cholesterol results from this device are at most risk.
Check the label for the lot number EL629. The product is a Wako HDL-C/LDL-C Calibrator used with Wako L-Type HDL-C or L-Type LDL-C for cholesterol testing.
Look for the lot number EL629 on the calibrator's label to confirm if it's affected.
The recall is due to incorrect concentration values printed on the label for Lot EL629, which may cause inaccurate cholesterol test results.
Check the label for the lot number EL629. The affected product is the Wako HDL-C/LDL-C Calibrator used with Wako L-Type HDL-C or L-Type LDL-C for cholesterol testing.
The official recall notice does not specify a remedy or action for affected units. Check the label for the lot number EL629 to confirm if it's affected.
We’ve drafted a message you can send Fujifilm to request your refund or repair — edit it as you like.
Subject: Recall Z-0932-2021 — Fujifilm Fujifilm Hello, I own a Fujifilm that is covered by recall Z-0932-2021 from Fujifilm. 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.
