Z-1683-2022 Class II Ongoing
FDA device recall Z-1683-2022 was initiated by Medline Industries Inc. on Jul 21, 2022 and is designated Class II. Reason for recall: Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit The recall status is ongoing. Affected quantity: 300 kits.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 14, 2022
- Initiation Date
- Jul 21, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 300 kits
Product Description
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
Distribution Pattern
U.S. Nationwide distribution in the state of AL.
Code Information
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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1683-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026