FDA Device recall Z-1287-2022
Medline Pill Splitters
- FDA Device
- Class II
- ongoing
- Published 2022-07-06
On 2022-07-06 the FDA classified a Class II recall of Medline Pill Splitters by Medline Industries Northfield, citing product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1287-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-05-11 |
| Published | 2022-07-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Medline Pill Splitters; 1 each/box; 144 boxes/carton
Reason
Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
Identifiers
| code_info | Model Number: NON135000; UDI/DI:8019673489; Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 5092104000…Model Number: NON135000; UDI/DI:8019673489; Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1287-2022%22
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