Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0 Recalled by CooperSurgical, Inc. Due to ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent

Date: March 27, 2019
Company: CooperSurgical, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact CooperSurgical, Inc. directly.

Affected Products

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

Quantity: 480 units

Why Was This Recalled?

ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent

Where Was This Sold?

Foreign: Denmark, Italy, Sweden

About CooperSurgical, Inc.

CooperSurgical, Inc. has 83 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report