BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166
Check against the official notice below — it lists the full affected range.
CareFusion has recalled BD MaxGuard Extension Sets with 0.2 Micron Filter and Needleless Y-Site (REF: MX9166) because the product labels incorrectly list an expiration year of 2027 when the actual expiration year should be 2025. The recall affects approximately 600 units with lot number 22029648 distributed across 43 U.S. states.
Using expired product could compromise the integrity of the extension set, potentially causing leaks and creating a risk of infection to both patients and healthcare workers. The source document does not specify a remedy or next steps 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: 600 Lot/code info: UDI-DI: 10885403237652, Lots: 22029648
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.