Perifix Continous Epidural Anesthesia Pain Control Trays; Injection of anesthetics to provide regional anesthesia for pain management.
Reported: October 28, 2015 Initiated: August 27, 2015 #Z-0150-2016
Product Description
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.
Details
- Recalling Firm
- B. Braun Medical, Inc.
- Units Affected
- 433
- Distribution
- Nationally
- Location
- Allentown, PA
Frequently Asked Questions
What product was recalled? ▼
Perifix Continous Epidural Anesthesia Pain Control Trays; Injection of anesthetics to provide regional anesthesia for pain management.. Recalled by B. Braun Medical, Inc.. Units affected: 433.
Why was this product recalled? ▼
Potential discoloration of the DuraPrep solution from unintended exposure to the sterilant during sterilization performed by the supplier.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 28, 2015. Severity: Moderate. Recall number: Z-0150-2016.
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