B Braun Medical Inc: Epidural Anesthesia Kit
Recall Summary B. Braun Medical Inc. is recalling epidural anesthesia kits distributed nationwide because the outside tubing may crack, making the kits unusable. The cracking issue comes from MASTISOL Liquid Adhesive, the component supplied by Ferndale Laboratories. The recall affects distribution in Alabama, Florida, Pennsylvania, Texas, Virginia, and Washington.
- Recalling firm
- B Braun Medical Inc
- Product
- Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Software Version: N/A Product Description: CESK SHANDS JACKSONVILLE 20055717 Component: No
- Reason
- B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-01-29
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2acf09f2-fb2d-4d92-bfa1-1caacc0de833