FDA Device recall Z-2229-2018
DermaPro Waterproof Silicone Tape, SNS57232
- FDA Device
- Class II
- terminated
- Published 2018-06-20
On 2018-06-20 the FDA classified a Class II recall of DermaPro Waterproof Silicone Tape, SNS57232 by Safe N Simple, citing the recalling firm received a customer complaint stating the tape was difficult to peel off the roll and had poor adhesion.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2229-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-12-14 |
| Published | 2018-06-20 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Safe N Simple |
| Distribution | AL, OH |
Product
DermaPro Waterproof Silicone Tape, SNS57232
Reason
The recalling firm received a customer complaint stating the tape was difficult to peel off the roll and had poor adhesion.
Identifiers
| code_info | 20170716. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2229-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.