SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG — Class II medical device recall Z-0660-2020
Terminated recall by Bellus Medical, reported 2019-12-18, distributed nationwide. Cosmetic Kit was packaged with a mislabel medical product.
| Recall number | Z-0660-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bellus Medical, Dallas, TX, United States |
| Recall initiated | 2019-01-18 |
| Classified | 2019-12-09 |
| Reported by FDA | 2019-12-18 |
| Terminated | 2021-03-05 |
| Distributed | Nationwide (US) |
| Quantity | 6,007 |
| Reason classes | labeling |
| Lot numbers | 16053 |
Product
SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Product Usage: The SKINFUSE Rescue Calming Complex is intend to be used to soothe and calm skin (cosmetic). The SKINFUSE LIFT HG is a hydrogel wound dressing to protect against abrasion and friction during the microneedling procedure.
Reason for recall
Cosmetic Kit was packaged with a mislabel medical product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0660-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.