NewDeal SA recalls UNI-CP devices with specific model numbers and lots due to risk of superficial or deep infections requiring antibiotics. Affected users should contact the manufacturer for details.
Use of the impacted product may cause a superficial infection requiring PO antibiotics and wound care or deep infection requiring IV antibiotics and device removal.
NewDeal SA is recalling UNI-CP devices with model numbers 330021S through 330430S to prevent infections that may require antibiotics. This recall is important because improper use could lead to infections needing medical treatment.
The recalled UNI-CP devices may cause infections that require antibiotics. Superficial infections might need oral antibiotics, while deeper infections could require intravenous antibiotics and device removal.
Users of UNI-CP devices with the listed model numbers and specific lots are affected. Individuals with these devices are at risk of infections requiring antibiotics.
Check the model number on your UNI-CP device. The affected models include 330021S, 330023S, 330025S, 330030S, 330217S, 330220S, 330225S, 330230S, 330420S, 330425S, and 330430S. Also check the lot number listed in the recall notice.
Identify your UNI-CP device's model number to see if it is listed in the recall.
Reach out to NewDeal SA for specific instructions on how to handle the device.
The affected model numbers are 330021S, 330023S, 330025S, 330030S, 330217S, 330220S, 330225S, 330230S, 330420S, 330425S, and 330430S.
Use of the impacted products may cause superficial infections requiring oral antibiotics or deep infections requiring intravenous antibiotics and device removal.
Check the model number on your device against the list provided in the recall notice and verify the lot number if it matches the specified lots.
We’ve drafted a message you can send NewDeal to request your refund or repair — edit it as you like.
Subject: Recall Z-2443-2018 — NewDeal NewDeal Hello, I own a NewDeal that is covered by recall Z-2443-2018 from NewDeal. 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.
