Class I — Medline Industries, LP
| 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 I |
| Status | Ongoing |
| Reason | Convenience kits labeled as sterile have not gone through the sterilization process. |
| Product | Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B |
| Quantity | 88 units |
| Distribution | US Distribution to States of: FL, MD, NJ, TN |
| Initiated | 2025-08-08 |
| Classified | 2025-09-26 |
| Recall number | Z-2593-2025 |
| 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 I recall — Medline Industries, LP (Z-2593-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97495/
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