BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141
Check against the official notice below — it lists the full affected range.
CareFusion has recalled BD MaxGuard Flow Controller Extension Sets (model MFS141) distributed across 40 U.S. states. The product labels incorrectly list the expiration year as 2027 when it should be 2025. A total of 37,550 units from lots 22029167, 22029168, and 22029169 are affected. The mislabeling creates a risk that expired products could be used in clinical settings, potentially compromising product integrity and resulting in leaks or infections for patients and healthcare workers.
The source does not specify a remedy or required action for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
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. Distribution: 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 Quantity: 37,550 Lot/code info: UDI-DI: 10885403236471, Lots: 22029167, 22029168, 22029169
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.