Medline recalls pill splitters with a lid that can come unhinged, exposing the blade. Affected units include specific model numbers and lot numbers. Stop using immediately to prevent injury.
Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
Medline is recalling pill splitters where the lid housing the blade can detach, exposing the sharp blade. This poses a risk of cuts or injuries if the splitter is used without the lid securely attached.
The product lid can become loose and detach from the base, exposing the blade. This means the sharp edge could cause cuts if the splitter is handled without the lid securely in place.
Pill splitters with model number NON135000 and specific lot numbers are affected. People using these splitters for medication are most at risk of injury.
Check for model number NON135000 and lot numbers listed: 50920060001 through 50922020001. These pill splitters were sold in cartons of 144 units.
Immediately stop using the pill splitter if the lid appears loose or detached.
Model number NON135000 with lot numbers 50920060001 through 50922020001.
Check for model number NON135000 and lot numbers listed: 50920060001 through 50922020001.
Stop using it immediately to prevent injury. The recall does not mention a replacement or repair option.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1287-2022 — Medline Medline Hello, I own a Medline that is covered by recall Z-1287-2022 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
