Device recall
Z-1249-2017: Durex Pleasure Pack. 3 ultra fine lubricated latex condoms 12 ultra fine…
FDA device recall · Class II · Reckitt Benckiser LLC
Key facts
| Recall number (Z-number) | Z-1249-2017 |
|---|---|
| Recall event | 75829 |
| 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) |
| Product code | HIS |
| Recalling firm | Reckitt Benckiser LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 15, 2020 |
| FEI number | 3011015568 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database