Medline Pill Splitters recall
Medline Pill Splitters; 1 each/box; 144 boxes/carton
Why was Medline Pill Splitters recalled?
Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
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: NON135000; UDI/DI:8019673489; Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001
- Product
- Medline Pill Splitters; 1 each/box; 144 boxes/carton
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 840,087 each
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, Singapore, Panama, and Hongkong.
- Recall date
- July 6, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)