Medline Open Heart recall
MEDLINE OPEN HEART, REF DYNJ904261B
Why was Medline Open Heart recalled?
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
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?
UDI/DI 40193489479530 (case), 10193489479539 (each), Lot Numbers: 23LBR364
- Product
- MEDLINE OPEN HEART, REF DYNJ904261B
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 30 units
- Distribution
- US Nationwide distribution.
- Recall date
- October 23, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)