Perifix¿ / Epidural anesthesia set recall: Labeling Error
Perifix¿ / Epidural anesthesia set, medicated
Why was Perifix¿ / Epidural anesthesia set recalled?
Product may be mislabeled with an incorrect lid stock label.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI-DI: 04046964178726 Product Code: 332250; Lot Number 0061863524, expiration date 30.APR.2025
- Product
- Perifix¿ / Epidural anesthesia set, medicated
- Recalling firm
- B. Braun Medical, Inc.
- Quantity
- 3440 units
- Distribution
- US Distributions to states of - AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA
- Recall date
- September 27, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)