B. Braun Medical, Inc. 2024-02-28 Health serious FDA
Health · FDA · Recall #FDA-Z-1150-2024
Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray… Recall
Issued February 28, 2024 · B. Braun Medical, Inc.
In February 2024, B. Braun Medical, Inc. recalled the Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Kits should contain Filter Straws with Standard Luer Connections however, the kits contain Filter Straws with Neuraxial connectors preventing interface with the other components of the kit.
What you should do
- 1 Stop using Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact B. Braun Medical, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- B. Braun Medical, Inc.
- Category
- Health
- Recall date
- February 28, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide
- Recall number
- FDA-Z-1150-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- B. Braun Medical, Inc. has 8 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.