Z-1555-2022 Class II Ongoing
FDA device recall Z-1555-2022 was initiated by Becton Dickinson & Company on Jul 18, 2022 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 9,340 units.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 24, 2022
- Initiation Date
- Jul 18, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9,340 units
Product Description
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.
Distribution Pattern
US Nationwide Distribution CA FL GA IL MD MI OR PA PR TN TX
Code Information
UDI-DI: 30382905153045 Lot Numbers: 2007212, 2103205
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1555-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026