Z-1287-2022 Class II Ongoing
FDA device recall Z-1287-2022 was initiated by MEDLINE INDUSTRIES, LP - Northfield on May 11, 2022 and is designated Class II. Reason for recall: Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade. The recall status is ongoing. Affected quantity: 840,087 each.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 6, 2022
- Initiation Date
- May 11, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 840,087 each
Product Description
Medline Pill Splitters; 1 each/box; 144 boxes/carton
Reason for Recall
Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Canada, Singapore, Panama, and Hongkong.
Code Information
Model Number: NON135000; UDI/DI:8019673489; Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1287-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026