CAREFUSION recalls BD MaxGuard Drop Administration sets with incorrect 2027 expiration labels (should be 2025). Using expired sets may cause leaks and infection risks. Affected units have specific lot numbers.
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 Drop Administration sets that have expiration labels showing 2027 instead of the correct 2025. Using these expired sets 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 expiration, the set may become compromised, causing leaks and increasing infection risks for patients and healthcare workers.
Healthcare workers and patients using the BD MaxGuard Drop Administration sets with incorrect expiration labels. Those most at risk are individuals using the sets for medical injections.
Check for BD MaxGuard Drop Administration sets with expiration labels showing 2027 (should be 2025). Affected units have lot numbers 22019074, 22019431, 22019075, or 22019076.
Look for expiration labels showing 2027 instead of 2025 on the BD MaxGuard Drop Administration set.
The product labels incorrectly list an expiration year of 2027 instead of 2025. Using expired sets may cause leaks and infection risks.
Check the expiration label on the product. If it shows 2027 instead of 2025, contact CAREFUSION for guidance.
Yes, affected units have lot numbers 22019074, 22019431, 22019075, or 22019076.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-1756-2022 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-1756-2022 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.
