MEDLINE INDUSTRIES, LP Northfield Medline Pill Splitters; 1 each/box; 144 boxes/carton Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medline Pill Splitters; 1 each/box; 144 boxes/carton
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
Model Number: NON135000, UDI/DI:8019673489, Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001
Products Sold
Model Number: NON135000; UDI/DI:8019673489; Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001
MEDLINE INDUSTRIES, LP Northfield is recalling Medline Pill Splitters; 1 each/box; 144 boxes/carton due to Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
Recommended Action
Per FDA guidance
The firm issued a recall notice to consignees on 05/11/2022 via mail. The letter instructs the consignee to check their stock, destroy affected product, and return the response form. On 5/16/2022, the firm sent out an updated recall notice.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026