Bellus Medical recalls SKINFUSE Rescue Calming Complex Kit that contains a mislabeled medical product. This cosmetic kit includes a hydrogel wound dressing intended for microneedling procedures.
Cosmetic Kit was packaged with a mislabel medical product.
Bellus Medical is recalling a SKINFUSE Rescue Calming Complex Kit that contains a hydrogel wound dressing (SKINFUSE LIFT HG) intended for medical use, not cosmetic. This mislabeling means the kit may be used incorrectly, potentially causing skin irritation or injury.
The kit contains a hydrogel wound dressing (SKINF: LIFT HG) designed for medical use during microneedling, not a cosmetic product. Using this in a cosmetic context could cause skin irritation, abrasions, or injury due to improper application.
People who purchased the SKINFUSE Rescue Calming Complex Kit from Bellus Medical. Those with sensitive skin or who use the kit for medical purposes are at higher risk of irritation or injury.
Check for the SKINFUSE Rescue Calming Complex Kit with the SKINFUSE LIFT HG hydrogel wound dressing tube. This product was sold by Bellus Medical and may have been purchased in 2023.
Look for the SKINFUSE LIFT HG hydrogel wound dressing tube inside the kit.
The recall states the kit contains a mislabeled medical product, so it may cause skin irritation or injury if used incorrectly.
The recall does not specify a remedy, so check the product label to confirm if it contains the SKINFUSE LIFT HG hydrogel wound dressing.
The product was recalled because it contains a hydrogel wound dressing intended for medical use, not a cosmetic product.
We’ve drafted a message you can send Bellus Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0660-2020 — Bellus Medical Bellus Medical Hello, I own a Bellus Medical that is covered by recall Z-0660-2020 from Bellus Medical. 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.
