BD MaxGuard Extension Set with 4-way stopcock (REF: M4058) has incorrect expiration year labels (2027 vs 2025). Using expired products may cause leaks and infection risks. Check labels for expiration year 2025.
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 recalled BD MaxGuard Extension Sets with 4-way stopcock (REF: M4:058) because their expiration year 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, but they should be 2025. If the product is used after expiration, it may become compromised, leading to leaks and infection risks for patients and healthcare workers.
Healthcare workers and patients using the BD MaxGuard Extension Sets with 4-way stopcock (REF: M4058) that have expiration year labels showing 2027 instead of 2025. Those using expired products face potential leaks and infection risks.
Check the product labels for expiration year 2027 instead of 2025. The product is the BD MaxGuard Extension Set with 4-way stopcock, REF: M4058, with UDI-DI: 10885403235788 and lots numbers 22019324, 22019323, 22019322.
Look for expiration year 2027 on the product label instead of 2025.
The product labels list an expiration year of 2027 but should list 2025. Using expired products may cause leaks and infection risks.
Check the expiration year on the label. If it shows 2027 instead of 2025, the product may be expired and could lead to leaks and infection risks.
The product is the BD MaxGuard Extension Set with 4-way stopcock, REF: M4058, with UDI-DI: 10885403235788 and lots numbers 22019324, 22019323, 22019322.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-1752-2022 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-1752-2022 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.
