BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059
Check against the official notice below — it lists the full affected range.
CareFusion has recalled BD MaxGuard Extension Sets with 2 Needleless Y-Site (REF: MX9059) because the product labels incorrectly list an expiration year of 2027 when the correct expiration year is 2025. A total of 17,250 units were distributed across 38 states, including Tennessee, Florida, Louisiana, Virginia, Michigan, Ohio, North Carolina, Washington, Utah, Texas, Nevada, Alabama, Arkansas, Iowa, Massachusetts, Colorado, New York, South Carolina, Indiana, Kentucky, Missouri, Maryland, Pennsylvania, California, Illinois, South Dakota, Georgia, Mississippi, Arizona, West Virginia, Idaho, Wyoming, Vermont, New Mexico, Oregon, New Jersey, Oklahoma, and Kansas. The affected lots are 22029431 and 22029432.
If expired product is used, the integrity of the administration and extension set may be compromised, potentially resulting in leaks and creating a risk of infection to both patients and healthcare workers. The recall record does not specify a remedy or instructions for what affected consumers should do.
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: 17,250 Lot/code info: UDI-DI: 10885403237584, Lots: 22029431, 22029432
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.