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 | Ongoing |
| Reason | Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit |
| Product | Medline CHEST TUBE REORDER NO: DYNJ36762A |
| Quantity | 300 kits |
| Distribution | U.S. Nationwide distribution in the state of AL. |
| Initiated | 2022-07-21 |
| Classified | 2022-09-07 |
| Recall number | Z-1683-2022 |
| 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-1683-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90689/
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