BARD MYPICC KIT 5F Triple-Lumen — Class II medical device recall Z-2076-2020
Terminated recall by Becton Dickinson & Company, reported 2020-05-27, distributed in IN, MO, OH, TX. The kits contain surgical gowns which were subject to a recall by the supplier.
| Recall number | Z-2076-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2020-02-26 |
| Classified | 2020-05-21 |
| Reported by FDA | 2020-05-27 |
| Terminated | 2020-09-22 |
| Distributed | IN, MO, OH, TX |
| Quantity | 1,262 total |
| Lot numbers | 18JBU370, 18OB4147, 19BBJ457 |
| Model numbers | CK000026A |
Product
BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000026A
Reason for recall
The kits contain surgical gowns which were subject to a recall by the supplier.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2076-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.