CAREF: BD MaxGuard 15 Drop Administration Sets with 2027 expiration labels may leak or cause infection if used after 2025. Recall details and action steps.
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.
CAREFUSION is recalling BD MaxGuard 15 Drop Administration Sets that have incorrect expiration labels showing 2027 instead of 2025. Using these expired products could lead to leaks and infection risks for patients and healthcare workers.
The product labels incorrectly list an expiration year of 2027 instead of 2025. If used after the correct expiration date, the product may become compromised, leading to potential leaks and infection risks for patients and healthcare workers.
Healthcare workers and patients using the BD MaxGuard 15 Drop Administration Sets with incorrect expiration labels. Those using the product after the 2025 expiration date are at risk of potential leaks and infection.
Check for BD MaxGuard 15 Drop Administration Sets with 4 Needleless Y-Sites, REF: MX9433. Labels show expiration year 2027 instead of 2025. Products were sold with UDI-DI: 10885403237782, Lots: 22019085.
Look for labels showing expiration year 2027 instead of 2025 on BD MaxGuard 15 Drop Administration Sets with REF: MX9433.
The product labels incorrectly list an expiration year of 2027 instead of 2025. Using expired products may lead to potential leaks and infection risks.
Check the expiration label on your BD MaxGuard 15 Drop Administration Set. If it shows 2027 instead of 2025, it is part of the recall.
The recall record does not mention a remedy or replacement option.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-1760-2022 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-1760-2022 from CAREFUSION. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
