CooperSurgical ICSI MicroPipette Recall: Missing 30-Degree Bend

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Recalling firmCooperSurgical, Inc.95 Corporate Dr, N/A · Trumbull, CT 06611-1350

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

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.

Why it’s dangerous

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.

Who’s affected

Users of ICSI MicroPipettes with part number MICC001-30-B1.0 are affected. Laboratory technicians and researchers using these pipettes are most at risk.

How to tell if you have this one

Check for the part number MICC001-30-B1.0 on the pipette. These units were sold in 2023 with lot number 1557.

Brand
CooperSurgical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the part number MICC001-30-B1.0 and lot number 1557 on the pipette.

✎ GovInfoNow

Questions people ask

What part number is recalled?

The recalled part number is MICC001-30-B1.0.

When were these units sold?

These units were sold in 2023.

Is there a fix for this issue?

The recall record does not mention a fix or remedy.

Take action

Contact CooperSurgical

We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.

✉️ Open in email

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.

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Where this comes from

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.

Official source: FDA Recall #Z-1367-2019 (March 27, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1367-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

CooperSurgical, Inc. recalls ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0

Lower-risk recall