CAREF: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site (REF MFS141) has expired label error. Labels show 2027 instead of 2025. Using expired product may cause leaks and infection risk.
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 Flow Controller Extension Sets (REF MFS141) because labels incorrectly show expiration year 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 the correct 2025. If the product is used after expiration, its integrity may be compromised, causing leaks and increasing infection risk for patients and healthcare workers.
Healthcare workers and patients using the BD MaxGuard Flow Controller Extension Set with Needleless Y-Site (REF MFS141) who have labels showing expiration year 2027 instead of 2025 are affected. Those using expired products face potential leaks and infection risks.
Check for BD MaxGuard Flow Controller Extension Sets with Needleless Y-Site (REF MFS141) that have labels showing expiration year 2027 instead of 2025. The product was sold with UDI-DI: 10885403236471 and lots: 22029167, 22029168, 22029169.
Verify the expiration year on the product label; it should be 2025, not 2027.
The product labels list an expiration year of 2027 instead of the correct 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 should not be used.
The recall does not provide a fix; the remedy is not stated in the record.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-1755-2022 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-1755-2022 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.
