BD PhaSealTM Y-Site Connector — Class II medical device recall Z-1555-2022
Ongoing recall by Becton Dickinson & Company, reported 2022-08-24, distributed nationwide. Incorrect expiration date listed on the product labels. The expiration date listed on the product label is bey
| Recall number | Z-1555-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2022-07-18 |
| Classified | 2022-08-18 |
| Reported by FDA | 2022-08-24 |
| Distributed | Nationwide (US) |
| Quantity | 9,340 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 30382905153045 |
| Lot numbers | 2007212, 2103205 |
| Model numbers | 515304 |
Product
BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the transfer of environmental contaminants into the system and the escape of drug or vapor concentrations outside the system. Catalog Number: 515304
Reason for recall
Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1555-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.