Perifix¿ / Epidural anesthesia set, medicated
Reported: September 27, 2023 Initiated: July 31, 2023 #Z-2627-2023
Product Description
Perifix¿ / Epidural anesthesia set, medicated
Reason for Recall
Product may be mislabeled with an incorrect lid stock label.
Details
- Recalling Firm
- B. Braun Medical, Inc.
- Units Affected
- 3440 units
- Distribution
- US Distributions to states of - AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA
- Location
- Allentown, PA
Frequently Asked Questions
What product was recalled? ▼
Perifix¿ / Epidural anesthesia set, medicated. Recalled by B. Braun Medical, Inc.. Units affected: 3440 units.
Why was this product recalled? ▼
Product may be mislabeled with an incorrect lid stock label.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 27, 2023. Severity: Moderate. Recall number: Z-2627-2023.
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