FDA Device recall Z-3001-2020
CVS Advanced Wart Remover Kit, Catalog Number: 1001-0407 - Product Usage: indicated for over-the-counter a cryosurgical system for the trea…
- FDA Device
- Class III
- terminated
- Published 2020-09-30
On 2020-09-30 the FDA classified a Class III recall of CVS Advanced Wart Remover Kit, Catalog Number: 1001-0407 - Product Usage: indicated for over-the-counter a cryosurgical system for the trea… by Orasure Technologies, citing unit boxes not properly sealed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3001-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2020-07-15 |
| Published | 2020-09-30 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Orasure Technologies |
| Distribution | US |
Product
CVS Advanced Wart Remover Kit, Catalog Number: 1001-0407 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of common warts and plantar warts.
Reason
Unit boxes not properly sealed
Identifiers
| code_info | Lot Numbers: 9214, 9256 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3001-2020%22
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