Medline Chest Tube Reorder No: Dynj36762a recall: Sterility Concern
Medline CHEST TUBE REORDER NO: DYNJ36762A
Why was Medline Chest Tube Reorder No: Dynj36762a recalled?
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- Medline CHEST TUBE REORDER NO: DYNJ36762A
- Recalling firm
- Medline Industries Inc.
- Quantity
- 300 kits
- Distribution
- U.S. Nationwide distribution in the state of AL.
- Recall date
- September 14, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)