DermaPro Waterproof Silicone Tape — Class II medical device recall Z-2229-2018
Terminated recall by Safe N Simple, LLC, reported 2018-06-20, distributed in AL, OH. The recalling firm received a customer complaint stating the tape was difficult to peel off the roll and had p
| Recall number | Z-2229-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Safe N Simple, LLC, Clarkston, MI, United States |
| Recall initiated | 2017-12-14 |
| Classified | 2018-06-14 |
| Reported by FDA | 2018-06-20 |
| Terminated | 2019-04-04 |
| Distributed | AL, OH |
| Quantity | 318 rolls |
Product
DermaPro Waterproof Silicone Tape, SNS57232
Reason for recall
The recalling firm received a customer complaint stating the tape was difficult to peel off the roll and had poor adhesion.
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-2229-2018. 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.