FDA DevicesClass II
Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY ...
Published: June 10, 2026Recall ID: Z-2270-2026Category: devicesCountry: US
Reason for Recall / Hazard
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.
Product Description & Identification
Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model/Catalog Number: 530134 Software Version: N/A Product Description: SESK UPMC DOUBLE CATHETER TRAY Component: No
Affected Products
Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model/Catalog Number: 530134 Software Version: N/A Product Description: SESK UPMC DOUBLE CATHETER TRAY Component: No
Additional Source Details
| Field | Value |
|---|---|
| City | Bethlehem |
| State | PA |
| Event id | 98862 |
| Address 1 | 824 12th Ave |
| Code info | Lot Code: Model No 530134, UDI-DI (Primary Device) 04046964305856, UDI-DI (Unit Device ID) 04046964305849, Lot Number 0062019148 |
| Postal code | 18018-3524 |
| Report date | 20260610 |
| Product type | Devices |
| Product quantity | 390 |
| Reason for recall | 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. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260129 |
| Initial firm notification | Letter |
| Center classification date | 20260529 |
Overview
- Recalling FirmB Braun Medical Inc
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.