Medical device recalls Moderate risk

CAREFUSION recalls BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433

Recall date
August 1, 2022
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1760-2022
FDA classification
Class II
Brand / firm
CAREFUSION
Sold / distributed
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

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433

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