BARD MYPICC Kit — Class II medical device recall Z-2378-2018
Terminated recall by Medline Industries, Inc., reported 2018-07-18, distributed in UT. One of the cases of product might not have been sterilized.
| Recall number | Z-2378-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, Inc., Waukegan, IL, United States |
| Recall initiated | 2018-01-12 |
| Classified | 2018-07-06 |
| Reported by FDA | 2018-07-18 |
| Terminated | 2020-07-22 |
| Distributed | UT |
| Lot numbers | 17YM5936 |
| Model numbers | CK000095B |
| Expiration dates | 2019-04-30 |
Product
BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures.
Reason for recall
One of the cases of product might not have been sterilized.
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-2378-2018. 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.