Z-2627-2023 Class II Ongoing
FDA device recall Z-2627-2023 was initiated by B. Braun Medical, Inc. on July 31, 2023 and is designated Class II. Reason for recall: Product may be mislabeled with an incorrect lid stock label. The recall status is ongoing. Affected quantity: 3440 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 27, 2023
- Initiation Date
- July 31, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3440 units
Product Description
Perifix¿ / Epidural anesthesia set, medicated
Reason for Recall
Product may be mislabeled with an incorrect lid stock label.
Distribution Pattern
US Distributions to states of - AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA
Code Information
UDI-DI: 04046964178726 Product Code: 332250; Lot Number 0061863524, expiration date 30.APR.2025