FDAClass IIAugust 18, 2021

Cutting Electrode Bipo 24.5fr recall

CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323

Why was Cutting Electrode Bipo 24.5fr recalled?

Product labeled as Cutting Electrode may contain BIVAP electrode.

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 21002858

Product
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
Recalling firm
Richard Wolf GmbH
Quantity
20 boxes
Distribution
US Nationwide Distribution in the states of CA, CO, IN, MA, NH
Recall date
August 18, 2021
Classification
Class II
Status
Terminated
Agency
FDA (device)
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