FDA Device recall Z-2081-2020
BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B
- FDA Device
- Class II
- terminated
- Published 2020-05-27
On 2020-05-27 the FDA classified a Class II recall of BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B by Becton Dickinson And, citing the kits contain surgical gowns which were subject to a recall by the supplier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2081-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-02-26 |
| Published | 2020-05-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | IN, MO, OH, TX |
Product
BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B
Reason
The kits contain surgical gowns which were subject to a recall by the supplier.
Identifiers
| code_info | Lot Numbers: 18OB4421 18PB2141 19CBK655 19FBJ721 19GBG835 19KBJ097 19TBD597 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2081-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.