FDAClass II · Medical device · Recall Z-2263-2026 · Recalled June 10, 2026

Brand Name recall — B Braun Medical Inc

Agency report date: June 10, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Brand Name
Company / brand: B Braun Medical
Lot / serial / date codes: Lot Code: Model No 555076, UDI-DI (Primary Device) 04046964313417, UDI-DI (Unit Device ID) 04046964313394, Lot Number 0062031523 Note: In the original customer notification (JAN2026), 280 pieces were distributed, to date, all pieces have been returned.
Distribution: US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

Agency product description and boundaries

Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Brand Name recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2263-2026
Brand: All B Braun Medical recalls
Classification: Class II
Units affected: 280
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Brand Name recall status

Companies & origin

Recalling firm location: Bethlehem, PA, United States
Firm address: 824 12th Ave, 18018-3524

Identifying details (verbatim from the notice)

Product codes / lots: Lot Code: Model No 555076, UDI-DI (Primary Device) 04046964313417, UDI-DI (Unit Device ID) 04046964313394, Lot Number 0062031523 Note: In the original customer notification (JAN2026), 280 pieces were distributed, to date, all pieces have been returned.
Distribution: US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.
Firm notified the public via: Letter
FDA event ID: 98862
Recall initiated: January 29, 2026
FDA classified: May 29, 2026
FDA report date: June 10, 2026

More B Braun Medical recalls

0 recall — B BRAUN MEDICAL INCFDA · September 16, 2026
Lactated Ringer's Injection USP recall — B BRAUN MEDICAL INCFDA · September 2, 2026
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits recall — B Braun Medical IncFDA · June 10, 2026
Spinocan Spinal Needle procedure kits recall — B Braun Medical IncFDA · June 10, 2026
Spinal Needle procedure kits recall — B Braun Medical IncFDA · June 10, 2026

Other medical device recalls from around the same time

Panda Freestanding Warmer recall — Datex-Ohmeda IncFDA · June 24, 2026
Giraffe Warmer with Integrated Resuscitation System (iRes) recall — Datex-Ohmeda IncFDA · June 24, 2026
Giraffe Stand-alone Infant Resuscitation System recall — Datex-Ohmeda IncFDA · June 24, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & CompanyFDA · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & CompanyFDA · June 10, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 8, 2026 at 6:00 PM UTC.

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