Medline CHEST TUBE REORDER NO: DYNJ36762A — Class II medical device recall Z-1683-2022
Ongoing recall by Medline Industries Inc., reported 2022-09-14, distributed nationwide. Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
| Recall number | Z-1683-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc., Laredo, TX, United States |
| Recall initiated | 2022-07-21 |
| Classified | 2022-09-07 |
| Reported by FDA | 2022-09-14 |
| Distributed | Nationwide (US) |
| Quantity | 300 kits |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 01019348989440, 40193489894401 |
| Lot numbers | 21ILA164, 21ILA986, 21JLA315, 21KLA005, 21KLA162, 21KLA629 |
| Model numbers | DYNJ36762A |
Product
Medline CHEST TUBE REORDER NO: DYNJ36762A
Reason for recall
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
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-1683-2022. 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.