Perifix Continous Epidural Anesthesia Pain Control Trays — Class II medical device recall Z-0150-2016
Terminated recall by B. Braun Medical, Inc., reported 2015-10-28. Potential discoloration of the DuraPrep solution from unintended exposure to the sterilant during sterilizatio
| Recall number | Z-0150-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | B. Braun Medical, Inc., Allentown, PA, United States |
| Recall initiated | 2015-08-27 |
| Classified | 2015-10-21 |
| Reported by FDA | 2015-10-28 |
| Terminated | 2016-06-29 |
| Quantity | 433 |
| Lot numbers | 0061413247, 0061414413, 0061416371, 0061416388, 0061416389, 0061417406, 0061420212, 0061421878 |
| Model numbers | 332215, 332262, 530024, 530132, 551714, 551879, 555184, 555259 |
Product
Perifix Continous Epidural Anesthesia Pain Control Trays; Injection of anesthetics to provide regional anesthesia for pain management.
Reason for recall
Potential discoloration of the DuraPrep solution from unintended exposure to the sterilant during sterilization performed by the supplier.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0150-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.