B. Braun Medical, Inc.: Medical Device Recall in 2016 - (Recall #: Z-1703-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units per case, Catalog Number 471734. Usage: Infusion of solution/medication into implanted intravascular ports.

Product Classification:

Class II

Date Initiated: April 26, 2016

Date Posted: June 1, 2016

Recall Number: Z-1703-2016

Event ID: 74171

Reason for Recall:

Potential for the tip of the Huber needle on the WHIN Infusion Set to protrude from the needle guard.

Status: Terminated

Product Quantity: 5,980 units [Lot # 0061482060 (3,340 units); Lot # 0061486821 (2,640 units)]

Code Information:

Catalog Number 471734, Lot Numbers: 0061482060 and 0061486821, expiration dates :1/31/2021 and 02/28/2021, respectively.

Distribution Pattern:

Worldwide distribution: US Distribution to states of: IN, NV, MA, IL, AR, TX, OH, CA, GA, FL, MS, NJ, AL, PA, TN, KY, VA, SC, and country of: Canada.

Voluntary or Mandated:

Voluntary: Firm initiated