Class II — Medline Industries, Inc.
| Recalling firm | Medline Industries, LP |
|---|---|
| Registered facility | View this company's 31 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | One of the cases of product might not have been sterilized. |
| Product | BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures. |
| Quantity | 6/5-kit cases |
| Distribution | The product was distributed to UT. |
| Initiated | 2018-01-12 |
| Classified | 2018-07-06 |
| Terminated | 2020-07-22 |
| Recall number | Z-2378-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medline Industries, Inc. (Z-2378-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80197/
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