FDA Device recall Z-1683-2022
Medline CHEST TUBE REORDER NO: DYNJ36762A
- FDA Device
- Class II
- ongoing
- Published 2022-09-14
On 2022-09-14 the FDA classified a Class II recall of Medline CHEST TUBE REORDER NO: DYNJ36762A by Medline Industries, citing due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1683-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-07-21 |
| Published | 2022-09-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline CHEST TUBE REORDER NO: DYNJ36762A
Reason
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
Identifiers
| code_info | Model Number: DYNJ36762A UDI-DI Code (GTIN Insert/GTIN Case / Lot Number: (01)1019348989440/(01)40193489894401 / 21ILA1…Model Number: DYNJ36762A UDI-DI Code (GTIN Insert/GTIN Case / Lot Number: (01)1019348989440/(01)40193489894401 / 21ILA164 (01)1019348989440/(01)40193489894401 / 21ILA986 (01)1019348989440/(01)40193489894401 / 21JLA315 (01)1019348989440/(01)40193489894401 / 21KLA005 (01)1019348989440/(01)40193489894401 / 21KLA162 (01)1019348989440/(01)40193489894401 / 21KLA629 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1683-2022%22
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