FDAClass IIIDecember 10, 2014

Cooper Surgical CANNULA-CURETTE 12MM recall

Cooper Surgical CANNULA-CURETTE 12MM; Model Number: MX562 The CooperSurgical SUCTION CANNULA-CURETTE device is used to remove tissue from within the…

Why was Cooper Surgical CANNULA-CURETTE 12MM recalled?

The product has been identified to contain an incorrect curette type.

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 Code: 147234

Product
Cooper Surgical CANNULA-CURETTE 12MM; Model Number: MX562 The CooperSurgical SUCTION CANNULA-CURETTE device is used to remove tissue from within the…
Recalling firm
CooperSurgical, Inc.
Quantity
30
Distribution
US Distribution including the states of NY, MO and NV.
Recall date
December 10, 2014
Classification
Class III
Status
Terminated
Agency
FDA (device)
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