B. Braun Medical, Inc. Perifix / Epidural anesthesia set, medicated Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Perifix / Epidural anesthesia set, medicated
Brand
B. Braun Medical, Inc.
Lot Codes / Batch Numbers
UDI-DI: 04046964178726 Product Code: 332250, Lot Number 0061863524, expiration date 30.APR.2025
Products Sold
UDI-DI: 04046964178726 Product Code: 332250; Lot Number 0061863524, expiration date 30.APR.2025
B. Braun Medical, Inc. is recalling Perifix / Epidural anesthesia set, medicated due to Product may be mislabeled with an incorrect lid stock label.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product may be mislabeled with an incorrect lid stock label.
Recommended Action
Per FDA guidance
An "URGENT MEDICAL DEVICE RECALL" letter dated 8/14/23 was issued to affected customers on 08/14/2023. The letter described the product, problem and actions to be taken. The Customers are instructed to review inventory, cease use and quarantine impacted product and complete and return the Product Recall Acknowledgement Form back to B. Braun Medical Inc. Quality Assurance department by faxing the form to (610)849-1197 or email to PA_QualityAssurance.BBMUS_Service@bbraunusa.com. B. Braun Medical will facilitate return of impacted product. If you have any questions, contact BBMI's Postmarket Surveillance Department at 1-833-425-1464.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, AR, CA, FL, GA, IL, MA, MO, NJ, NC, PA, TX, WA
Page updated: Jan 10, 2026