PlainRecalls
FDA Devices Moderate Class II Terminated

CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323

Reported: August 18, 2021 Initiated: June 25, 2021 #Z-2246-2021

Product Description

CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323

Reason for Recall

Product labeled as Cutting Electrode may contain BIVAP electrode.

Details

Recalling Firm
Richard Wolf GmbH
Units Affected
20 boxes
Distribution
US Nationwide Distribution in the states of CA, CO, IN, MA, NH
Location
Knittlingen, N/A

Frequently Asked Questions

What product was recalled?
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323. Recalled by Richard Wolf GmbH. Units affected: 20 boxes.
Why was this product recalled?
Product labeled as Cutting Electrode may contain BIVAP electrode.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 18, 2021. Severity: Moderate. Recall number: Z-2246-2021.