Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1482-2026 — Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air o

U.S. FDA — Device Enforcement · United States · 2026-02-02 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1482-2026
Date of alert: 2026-02-02
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: B Braun Medical Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 4046964338434

Reported risk: The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related