CLASS II ONGOING Device recall · Reported 10 Jun 2026 · FDA Enforcement Report

Cesk Riverside Health System recalled by B Braun Medical

B Braun Medical is recalling Cesk Riverside Health System, distributed nationwide in the US. The recall was initiated on 29 Jan 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: Model No 552126, UDI-DI (Primary Device) 04046955056903, UDI-DI (Unit Device ID) 04046955056897, Lot Number 0062031274

Quantity recalled690

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2268-2026
FDA event ID: 98862
Recalling firm: B Braun Medical, Bethlehem, PA
Classification: Class II
Status: Ongoing
Recall initiated: 29 Jan 2026
FDA classified: 29 May 2026
Reported: 10 Jun 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Device Malfunction
Device type: Medical Software

Timeline

29 Jan 2026	Recall initiated by company
29 May 2026	Classified by FDA	+120 days
10 Jun 2026	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM Model/Catalog Number: 552126 Software Version: N/A Product Description: CESK RIVERSIDE HEALTH SYSTEM Component: No

Where it was distributed

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

Nationwide Alabama Florida Pennsylvania Texas Virginia Washington

Questions about this recall

Why was it recalled?

Which lots are affected?

Lot Code: Model No 552126, UDI-DI (Primary Device) 04046955056903, UDI-DI (Unit Device ID) 04046955056897, Lot Number 0062031274

Where was it sold?

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

7 other products · FDA event 98862

This product is part of a recall event; the main page for the event is Cesk Harris Methodist recalled by B Braun Medical.

Reported	Class	Recall	Company	Reason	Where
10 Jun 2026	CLASS II	Cesk Harris Methodist recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide
10 Jun 2026	CLASS II	Cesk Northside Anesthesia Tray recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide
10 Jun 2026	CLASS II	Cesk Shands Jacksonville recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide
10 Jun 2026	CLASS II	Nes1725kfxl Spinal Epid Closed Tip Cath recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide
10 Jun 2026	CLASS II	Bpsk, Blockjocks Tray recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide
10 Jun 2026	CLASS II	Lyndon B Johnson Hospital Spinal Epid recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide
10 Jun 2026	CLASS II	Sesk Upmc Double Catheter Tray recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide

More recalls from B Braun Medical

All 447

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3 Sep 2026Drug	ANNOUNCED	B. Braun 0.9% Sodium Chloride Injection USP, in a PAB Container recalledB. Braun	B. Braun Medical	Particulate Matter	Nationwide
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10 Jun 2026Device	CLASS I	Design Options Spinal Tray Spinal Needle Anesthesia recalled	B Braun Medical	Processing Deviation	Nationwide
10 Jun 2026Device	CLASS II	Sesk Upmc Double Catheter Tray recalled by B Braun Medical	B Braun Medical	Device Malfunction	Nationwide

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