Recall Z-2627-2023— B. Braun Medical, Inc.
Class II · Ongoing
Class II FDA medical device recall by B. Braun Medical, Inc., initiated 2023-07-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Perifix¿ / Epidural anesthesia set, medicated. Reason: Product may be mislabeled with an incorrect lid stock label..
- Recalling firm
- B. Braun Medical, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-07-31
- Firm location
- Allentown, PA, United States
Product description
Perifix¿ / Epidural anesthesia set, medicated
Reason for recall
Product may be mislabeled with an incorrect lid stock label.
Data sourced from openFDA. This site is unofficial and independent of the FDA.