Z-2165-2013 Class II Terminated
FDA device recall Z-2165-2013 was initiated by Baxa Corporation on August 22, 2013 and is designated Class II. Reason for recall: Baxter Healthcare Corporation is voluntarily recalling one lot of Baxa Vial Adapters, 14mm - Luer Lock, due to incorrect expiry date. The recall status is terminated (terminated August 19, 2016). Affected quantity: 34 cases.
Recall Details
- Product Type
- Devices
- Report Date
- September 18, 2013
- Initiation Date
- August 22, 2013
- Termination Date
- August 19, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 34 cases
Product Description
Baxa Vial Adapter, 14mm - Luer Lock, Order No. REF: 90, Quantity: 50 each, Single Use. Product Code H93890. Used as a needleless access device for reconstitution and drug transfer.
Reason for Recall
Baxter Healthcare Corporation is voluntarily recalling one lot of Baxa Vial Adapters, 14mm - Luer Lock, due to incorrect expiry date.
Distribution Pattern
Distributed to One Customer in NC.
Code Information
Lot or Serial No. 785518