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
Reported: August 24, 2022 Initiated: July 18, 2022 #Z-1555-2022
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.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 9,340 units
- Distribution
- US Nationwide Distribution CA FL GA IL MD MI OR PA PR TN TX
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Becton Dickinson & Company. Units affected: 9,340 units.
Why was this product recalled? ▼
Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 24, 2022. Severity: Moderate. Recall number: Z-1555-2022.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11