Medline Pill Splitters — Class II medical device recall Z-1287-2022
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2022-07-06, distributed nationwide. Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
| Recall number | Z-1287-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2022-05-11 |
| Classified | 2022-06-24 |
| Reported by FDA | 2022-07-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, PA, SG |
| Quantity | 840,087 units |
| Lot numbers | 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001 |
| Model numbers | NON135000 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1287-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.