FDAClass IIMay 29, 2019

ICSI MICROPIPETTE CooperSurgical recall

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

Why was ICSI MICROPIPETTE CooperSurgical recalled?

ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot 1557

Product
ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
Recalling firm
CooperSurgical, Inc.
Quantity
480 units
Distribution
Foreign: Denmark, Italy, Sweden
Recall date
May 29, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls