Z-2246-2021 Class II Terminated
FDA device recall Z-2246-2021 was initiated by Richard Wolf GmbH on Jun 25, 2021 and is designated Class II. Reason for recall: Product labeled as Cutting Electrode may contain BIVAP electrode. The recall status is terminated (terminated Jan 5, 2024). Affected quantity: 20 boxes.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 18, 2021
- Initiation Date
- Jun 25, 2021
- Termination Date
- Jan 5, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 20 boxes
Product Description
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
Reason for Recall
Product labeled as Cutting Electrode may contain BIVAP electrode.
Distribution Pattern
US Nationwide Distribution in the states of CA, CO, IN, MA, NH
Code Information
Lot Number 21002858
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2246-2021
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026