CAREFUSION: Medical Device Recall in 2022 - (Recall #: Z-1759-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171

Product Classification:

Class II

Date Initiated: August 1, 2022

Date Posted: September 28, 2022

Recall Number: Z-1759-2022

Event ID: 90707

Reason for Recall:

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Status: Ongoing

Product Quantity: 100

Code Information:

UDI-DI: 10885403237669, Lots: 22029674

Distribution Pattern:

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

Voluntary or Mandated:

Voluntary: Firm initiated