CAREFUSION recalls BD MaxGuard Extension Set (REF: ME1069) due to incorrect expiration label (2027 listed instead of 2025). Using expired products may cause leaks and infection risks for patients and healthcare workers.
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: BD MaxGuard Extension Sets with incorrect expiration labels (showing 2027 instead of 2025) are being recalled. Using these expired products 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 the product is used after the actual expiration date (2025), 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 (REF: ME1069) with expiration labels showing 2027 instead of 2025 are affected. Those who have used the product after the correct expiration date (2025) are at higher risk.
Check the expiration label on the BD MaxGuard Extension Set (REF: ME1069) for the year 2027 instead of 2025. The product was sold with UDI-DI: 10885403236037 and lot number 22019062.
Look for the expiration label showing 2027 instead of 2025 on the BD MaxGuard Extension Set (REF: ME1069).
The product labels incorrectly list an expiration year of 2027 instead of 2025. Using expired products may cause leaks and infection risks.
Check the expiration label for 2027 instead of 2025. If it shows 2027, contact CAREFUSION for guidance.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-1753-2022 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-1753-2022 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.
