B Braun Medical Inc: Medical Device Recall in 2026 - (Recall #: Z-1482-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

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 or fluids. Component: N/A

Product Classification:

Class II

Date Initiated: February 2, 2026

Date Posted: March 11, 2026

Recall Number: Z-1482-2026

Event ID: 98380

Reason for Recall:

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

Status: Ongoing

Product Quantity: 21000 units

Code Information:

Model/Catalog Number: 7A3842; Primary-DI 4046964338434; Unit of Use- DI 4046964338410; Lot 0062004706, Exp 31MAR2032; Lot 0062005799, Exp 30JUN2032; Lot 0062006415, Exp 31MAR2032; Lot 0062006416, Exp 31MAR2032; Lot 0062023397, Exp 30JUN2032; Lot 0062024887, Exp 31JUL2032

Distribution Pattern:

Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.

Voluntary or Mandated:

Voluntary: Firm initiated