Class II — Reckitt Benckiser LLC
| Recalling firm | Reckitt Benckiser LLC |
|---|---|
| Registered facility | View this company's 5 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The products failed the filed specification of 1.0kPa for Burst Pressure. |
| Product | Durex Real Feel Polyisoprene Condoms, 10 count and 24 count, SKU Numbers 02340-89456-14 and 02340-89457-00 Product Usage: The Durex Synthetic polyisoprene male condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted disease). |
| Quantity | 487980 condoms |
| Distribution | US Nationwide. |
| Initiated | 2018-07-23 |
| Classified | 2018-09-24 |
| Terminated | 2020-03-05 |
| Recall number | Z-3241-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Reckitt Benckiser LLC (Z-3241-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80841/
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