BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock, REF: MX4436
Check against the official notice below — it lists the full affected range.
CareFusion has recalled 19,925 BD MaxGuard Drop Administration sets with 3 Needleless Y-Sites and removable manifolds distributed across 39 U.S. states. The product labels incorrectly list an expiration year of 2027 when the actual expiration year is 2025. If expired product is used, the integrity of the product may be compromised, potentially resulting in leaks and increasing the risk of infection to patients and healthcare workers.
The affected products are identified by UDI-DI 10885403237478 and lot numbers 22019074, 22019431, 22019075, and 22019076. The source document does not specify what remedy consumers or healthcare facilities should take.
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: 19,925 Lot/code info: UDI-DI: 10885403237478, Lots: 22019074, 22019431, 22019075, 22019076
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.