Copan Diagnostics recalls 1000-pc sets of 300uL transfer pipettes with plastic defects that could cause inaccurate measurements. Affected units have specific lot codes and UDI numbers. Consumers should contact Copan for details.
Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance
Copan Diagnostics is recalling 1000-pc sets of 300uL transfer pipettes due to plastic defects that might cause inaccurate measurements. This could affect lab work requiring precise fluid handling.
The plastic defects may cause the pipette to not measure fluids accurately. This could lead to incorrect results in lab experiments or medical testing where precise measurements are critical.
Users of lab equipment who purchased these pipettes from specific lot codes or UDI numbers. Researchers and technicians working with precise fluid measurements are most at risk.
Check for the UDI number 50841467100545 or lot codes listed: B104661, B202918, B203404, B203405, B204186, B204187, B204819, B204820, B300133, B300410, B300608, B300647, B300679, B301129, B301133, B301135, B301134.
Look for the UDI number 50841467100545 or the listed lot codes on the packaging.
The plastic defects may cause the pipette to not measure fluids accurately, potentially affecting lab results.
Check for the UDI number 50841467100545 or lot codes: B104661, B202918, B203404, B203405, B204186, B204187, B204819, B204820, B300133, B300410, B300608, B300647, B300679, B301129, B301133, B301135, B301134.
The recall does not specify a remedy, so contact Copan Diagnostics directly for further instructions.
We’ve drafted a message you can send Copan Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-2620-2023 — Copan Diagnostics Copan Diagnostics Hello, I own a Copan Diagnostics that is covered by recall Z-2620-2023 from Copan Diagnostics. 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.
