Willa Pore Perfector — Class II drug recall D-0093-2021
Terminated recall by Milbar Laboratories, Inc., reported 2020-11-25, distributed nationwide. GMP Deviations
| Recall number | D-0093-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Milbar Laboratories, Inc., East Haven, CT, United States |
| Recall initiated | 2020-10-09 |
| Classified | 2020-11-17 |
| Reported by FDA | 2020-11-25 |
| Terminated | 2023-01-04 |
| Distributed | Nationwide (US) |
| Quantity | 2,638 plastic |
| Reason classes | cgmp |
| Lot numbers | CW828-0, MAR-22 |
Product
Willa Pore Perfector (Salicylic Acid 2%) pads, 30 pads
Reason for recall
GMP Deviations
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/D-0093-2021. 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.