CAREFUSION recalls BD MaxGuard Extension Sets with 2027 expiration labels instead of 2025. Using expired products may cause leaks and infection risks. Check your product's label for expiration year.
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.
CAREF:USION recalled BD MaxGuard Extension Sets that incorrectly list 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, it may become compromised, causing leaks and increasing infection risks for patients and healthcare workers.
Healthcare workers and patients using the BD MaxGuard Extension Sets with the 2027 expiration label instead of 2025. Those with the specific model number and lot code are most at risk.
Check the product label for the expiration year. The correct expiration year is 2025, but the labels list 2027. The product model is BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166.
Look for 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 product label for the expiration year. If it lists 2027 instead of 2025, contact CAREFUSION for guidance.
The recall record does not mention any remedy or replacement options.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-1758-2022 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-1758-2022 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.
