FDAClass IIMay 23, 2018

Fischer Cone Biopsy Excisor recall

Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151

Why was Fischer Cone Biopsy Excisor recalled?

Products have been packaged with an incorrect product size.

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 number: 212074

Product
Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
Recalling firm
CooperSurgical, Inc.
Quantity
500
Distribution
CA, SC, WI, MI, NH, MD, OH, NJ, Australia, France, Spain
Recall date
May 23, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls