B Braun Medical Inc: Medical Device Recall in 2026 - (Recall #: Z-1483-2026)

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 INF SET Model/Catalog Number: 7M2802 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-1483-2026

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: 51300 units

Code Information:

Model/Catalog Number: 7M2802; Primary-DI 4046964787102, Unit of Use- DI 4046964349904; Lot 0062003864, Exp 30APR2032; Lot 0062004133, Exp 30JUN2032; Lot 0062006454, Exp 31JUL2032; Lot 0062028929, Exp 31AUG2032; Lot 0062037141, Exp 30SEP2032, Lot 0062037691, Exp 30SEP2032.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated