Home/Recalls/FDA-Z-2270-2026
FDA DevicesClass II

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

Published: June 10, 2026Recall ID: Z-2270-2026Category: devicesCountry: US
US
Medical DeviceFDA DevicesUSUS

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

Recalling Firm: B Braun Medical Inc

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

FieldValue
CityBethlehem
StatePA
Event id98862
Address 1824 12th Ave
Code infoLot Code: Model No 530134, UDI-DI (Primary Device) 04046964305856, UDI-DI (Unit Device ID) 04046964305849, Lot Number 0062019148
Postal code18018-3524
Report date20260610
Product typeDevices
Product quantity390
Reason for recallB. 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 mandatedVoluntary: Firm initiated
Recall initiation date20260129
Initial firm notificationLetter
Center classification date20260529

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Overview

  • Recalling FirmB Braun Medical Inc
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.
Recall Hazard Severity
High Alert (Class I)
Official Agency Alert

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