CooperSurgical recalls ICSI MicroPipettes with part number MICC001-30-B1.0 due to missing 30-degree bend. Affected units sold in 2023.
ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
CooperSurgical is recalling ICSI MicroPipettes with part number MICC0:30-B1.0 because they lack a 30-degree bend. This could cause the pipette to bend or break unexpectedly during use.
The pipette lacks a 30-degree bend, which is designed to prevent sharp bends during use. Without this feature, the pipette may bend or break unexpectedly, potentially causing injury or inaccurate measurements.
Users of ICSI MicroPipettes with part number MICC001-30-B1.0 are affected. Laboratory technicians and researchers using these pipettes are most at risk.
Check for the part number MICC001-30-B1.0 on the pipette. These units were sold in 2023 with lot number 1557.
Look for the part number MICC001-30-B1.0 and lot number 1557 on the pipette.
The recalled part number is MICC001-30-B1.0.
These units were sold in 2023.
The recall record does not mention a fix or remedy.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1367-2019 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-1367-2019 from CooperSurgical. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
