Valeritas recalls 20-unit demo cartons with possible needle inclusion. Consumers should check product labels for part number 2568-03 and lot number DM218024 to avoid potential injury risks.
There is a potential for "No Needle Demo Units" to contain a needle.
Valer:itas is recalling demo cartons that may contain needles. This poses a risk of injury if someone accidentally handles the carton without proper care.
The carton is designed to be a demo unit without needles, but there's a potential for needles to be included. If a needle is present, it could cause injury if touched or handled improperly.
Anyone who owns or uses the DEMO No Needle Corrugated Carton 20 U/D with part number 2568-03. People handling the carton without checking for needles are most at risk.
Look for the carton labeled 'DEMO No Needle Corrugated Carton 20 U/D' with part number 2568-03 and lot number DM218024. Check the carton's unique identifier (UDI) code on the label.
Look for the part number 2568-03 and lot number DM218024 on the carton's label to confirm it's the recalled item.
The recall states there's a potential for needles to be included, so it's not safe to use without checking for needles.
Check the carton label for part number 2568-03 and lot number DM218024.
The recall doesn't specify a remedy, so you should check the carton label to confirm and avoid handling it if needles are present.
We’ve drafted a message you can send Valeritas to request your refund or repair — edit it as you like.
Subject: Recall Z-0198-2020 — Valeritas Valeritas Hello, I own a Valeritas that is covered by recall Z-0198-2020 from Valeritas. 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.
