Lower riskMedical device recall · FDA · Published July 18, 2022
BD PhaSe: Y-Site Connector Recall: Incorrect Expiration Date on Labels
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.
Take action
Contact the company
📍Recalling firmBecton Dickinson & Company1 Becton Dr · Franklin Lakes, NJ 07417-1815
✎ GovInfoNow plain-language explainer
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. Read more at govinfonow.com/recall/60358-bd-phase-y-site-connector-recall-incorrect-expiration-date-on.
“BD PhaSe: Y-Site Connector Recall: Incorrect Expiration Date on Labels.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60358-bd-phase-y-site-connector-recall-incorrect-expiration-date-on. Based on FDA recall #Z-1555-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1555-2022%22&limit=1).
Becton Dickinson & Company recalled BD PhaSealTM Y-Site Connector (C80) Closed System Drug Transfer Devices due to incorrect expiration dates on labels, the FDA announced July 18, 2022. Owners should check lot numbers and contact the company for a remedy.
How to tell if you have it
Brand: Becton Dickinson
Product: BD PhaSealTM Y-Site Connector (C80)
Catalog Number: 515304
UDI-DI: 30382905153045
Lot Numbers: 2007212, 2103205
Units affected: 9,340
The hazard
The hazard is an incorrect expiration date listed on the product labels. The expiration date listed on the label is beyond the actual expiration date of the product.
Context
GovInfoNow's records show Becton Dickinson & Company has 52 other recalls on record since May 31, 2017. Other recent recalls include a spinal tray recall due to quality issues (April 27, 2026), non-sterile Luer-Lok syringes recalled for wrong type (Jan. 27, 2026), and Luer tip caps recalled for failed biocompatibility testing (Oct. 14, 2025). Other recent recalls of similar products include a B Braun Discofix Four Way Stopcock recall for incorrect expiration date on carton (Aug. 4, 2026), a BD Ready-to-Use Hydrophilic Catheter 14 Fr recall for incorrect expiration date labeling (Nov. 29, 2025), and a Cook Medical Spectrum Central Venous Tray recall for expiration dates exceeding shelf life (March 5, 2026).
How to tell if you have this one
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.
Brand
Becton Dickinson
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Expiration Date
Verify the expiration date on the product label matches the actual expiration date of the device.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 10 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide Distribution CA FL GA IL MD MI OR PA PR TN TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, Georgia, Illinois, Maryland, Michigan, Oregon, Pennsylvania, Puerto Rico, Tennessee, Texas.
Recall timeline
FDA published this recall 37 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-1555-2022 (July 18, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1555-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.