Becton Dickinson recalls BD PhaSeal Y-Site Connectors with incorrect expiration dates on labels. These devices may expire before use, risking medication safety. Affected units include specific lot numbers.
Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
Becton Dickinson is recalling BD PhaSeal Y-Site Connectors (C80) due to incorrect expiration dates on labels. This could mean the product expires before it's used, potentially leading to medication safety issues. Affected units have specific lot numbers.
The product labels list an expiration date that is beyond the actual expiration date of the product. This means the device might expire before it's used, potentially leading to medication safety issues.
Healthcare professionals using these connectors for drug transfers are most at risk. Patients receiving medication through these devices could be affected if the expiration date is incorrect.
Check for the product name 'BD PhaSeal Y-Site Connector (C80)' and lot numbers 2007212 or 2103205. These are the specific units affected by the recall.
Verify the expiration date on the product label matches the actual expiration date of the device.
The product labels list an expiration date that is beyond the actual expiration date of the product, which could mean the device expires before it's used.
Lot numbers 2007212 and 2103205 are affected by this recall.
Check for the product name 'BD PhaSeal Y-Site Connector (C80)' and lot numbers 2007212 or 2103205.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1555-2022 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1555-2022 from Becton Dickinson. 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.
