NewDeal SA recalls Large QWIX models 111740S-121820S due to risk of infection requiring antibiotics. Affected units include specific model numbers and lot codes.
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 Large QWIX products with model numbers 111740S through 121820S because they may cause infections that require antibiotics. This recall affects users who own these specific models and lot numbers.
The recalled Large QWIX products may cause infections that require antibiotics. Infections could range from superficial (requiring oral antibiotics) to deep (requiring intravenous antibiotics and device removal).
Users of the Large QWIX products with model numbers 111740S through 121820S and specific lot codes are affected. Those with these models and lot numbers are most at risk.
Check if your Large QWIX has a model number starting with 111740S through 121820S. Look for specific lot codes listed in the recall notice.
Identify your Large QWIX model number from the product label to see if it is in the list of affected models (111740S through 121820S).
Find the lot code on your product label and compare it to the specific lot codes listed in the recall notice.
The recall does not require immediate stop use. You can continue using the product but should check if it is affected before taking action.
The recall does not specify a remedy. Affected units may need to be checked for infections, but no specific action is required beyond identifying the product.
Check the model number on your product label to see if it is in the range 111740S through 121820S and compare the lot code to the specific lot codes listed in the recall notice.
We’ve drafted a message you can send NewDeal to request your refund or repair — edit it as you like.
Subject: Recall Z-2446-2018 — NewDeal NewDeal Hello, I own a NewDeal that is covered by recall Z-2446-2018 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.
