FDA Device recall Z-0150-2016
Perifix Continous Epidural Anesthesia Pain Control Trays
- FDA Device
- Class II
- terminated
- Published 2015-10-28
On 2015-10-28 the FDA classified a Class II recall of Perifix Continous Epidural Anesthesia Pain Control Trays by B Braun Medical, citing potential discoloration of the DuraPrep solution from unintended exposure to the sterilant during sterilization performed by the supplier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0150-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-27 |
| Published | 2015-10-28 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | B Braun Medical |
| Distribution | n/a |
Product
Perifix Continous Epidural Anesthesia Pain Control Trays; Injection of anesthetics to provide regional anesthesia for pain management.
Reason
Potential discoloration of the DuraPrep solution from unintended exposure to the sterilant during sterilization performed by the supplier.
Identifiers
| code_info | Product Catalog Number: 332215 332262 530024 530132 551714 551879 555184 555259 Lot Number 0061417406 006142…Product Catalog Number: 332215 332262 530024 530132 551714 551879 555184 555259 Lot Number 0061417406 0061421878 0061416371 0061420212 0061413247 0061416388 0061416389 0061414413 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0150-2016%22
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