Durex Pleasure Pack — Class II medical device recall Z-1249-2017
Terminated recall by Reckitt Benckiser LLC, reported 2017-03-01, distributed nationwide. Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labe
| Recall number | Z-1249-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Reckitt Benckiser LLC, Parsippany, NJ, United States |
| Recall initiated | 2016-11-22 |
| Classified | 2017-02-23 |
| Reported by FDA | 2017-03-01 |
| Terminated | 2020-01-15 |
| Distributed | Nationwide (US) |
| Quantity | 108,342 units |
| Reason classes | labeling |
| Model numbers | 02340-30042-04, 02340-302190-04, 02340-30274-08, 02340-70042-04 |
Product
Durex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated latex condoms 24 Ra fine lubricated latex condoms 3 ct UPC 3-02340-30042-04-1 3 ct - Walmart UPC 02340-70042-04 12ct - UPC 3-02340-30274-08-6 24 ct - UPC 302340-302190-04 (contacting firm for label)
Reason for recall
Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.
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-1249-2017. 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.