CAREFUSION recalls BD MaxGuard Extension Set with 2 Needleless Y-Site (REF: MX905: 2027 label error may cause leaks and infection risk if expired.
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 recalls BD MaxGuard Extension Sets with 2 Needleless Y-Site (REF: MX9059) because their expiration labels show 2027 instead of 2025. Using expired products could lead to leaks and infection risks for patients and healthcare workers.
The product labels list an expiration year of 2027 instead of 2025. If the product is expired, it may become compromised, leading to potential leaks and infection risks for patients and healthcare workers.
Healthcare workers and patients using the BD MaxGuard Extension Set with 2 Needleless Y-Site (REF: MX9059) that have labels showing expiration year 2027 instead of 2025.
Check for BD MaxGuard Extension Sets with 2 Needleless Y-Site (REF: MX9059) that have labels showing expiration year 2027 instead of 2025. The product was sold with UDI-DI: 10885403237584 and lots 22029431, 22029432.
Verify the expiration year on the product label; it should read 2025, not 2027.
The product labels list an expiration year of 2027 instead of 2025. Using expired products could lead to leaks and infection risks.
Check the expiration year on the label; it should read 2025. If it shows 2027, the product may be compromised and could lead to leaks and infection risks.
Look for BD MaxGuard Extension Sets with 2 Needleless Y-Site (REF: MX9059) with UDI-DI: 10885403237584 and lots 22029431 or 22029432.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-1757-2022 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-1757-2022 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.
