Perifix¿ / Epidural anesthesia kit recall
Perifix¿ / Epidural anesthesia kit (10 count carton)
Why was Perifix¿ / Epidural anesthesia kit recalled?
Kits were assembled with the incorrect Filter Straw.
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?
Model No. 332217, 332097, 332220, 332078; GTIN: 04046964178283, 04046964177361, 04046964177361, 04046964178320, 04046964177200; Lot No. 0061850767, 0061855339, 00618553400061858554, 0061837264.
- Product
- Perifix¿ / Epidural anesthesia kit (10 count carton)
- Recalling firm
- B. Braun Medical, Inc.
- Quantity
- 16,070 units
- Distribution
- US Nationwide distribution.
- Recall date
- July 5, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)