Z-2080-2020 Class II Terminated
FDA device recall Z-2080-2020 was initiated by Becton Dickinson & Company on February 26, 2020 and is designated Class II. Reason for recall: The kits contain surgical gowns which were subject to a recall by the supplier. The recall status is terminated (terminated September 22, 2020). Affected quantity: 1262 total.
Recall Details
- Product Type
- Devices
- Report Date
- May 27, 2020
- Initiation Date
- February 26, 2020
- Termination Date
- September 22, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1262 total
Product Description
BARD MYPICC KIT 3F Single-Lumen, Catalog Number CK000417B
Reason for Recall
The kits contain surgical gowns which were subject to a recall by the supplier.
Distribution Pattern
The products were distributed to the following US states: IN, MO, OH, and TX.
Code Information
Lot Numbers: 18KBN221 18MB9962 18NB2698 19FBK323 19LBB569 19SBH078 19TBD608