Drug recall
Durex Pleasure Pack. 3 ultra fine lubricated latex condoms 12 ultra fine lubricated latex condoms 24 Ra fine…
FDA recall event 75829 · Class II · Reckitt Benckiser LLC
Key facts
| Event ID | 75829 |
|---|---|
| Recall numbers | Z-1249-2017 |
| Recalling firm | Reckitt Benckiser LLC |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Nov 22, 2016 |
| Report date | Mar 1, 2017 |
| Termination date | Jan 15, 2020 |
| City | Parsippany |
| State | NJ |
| Country | United States |
| FEI number | 3011015568 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: