Device recall
Z-0994-2019: Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU…
FDA device recall · Class II · Reckitt Benckiser LLC
Key facts
| Recall number (Z-number) | Z-0994-2019 |
|---|---|
| Recall event | 81964 |
| Product | Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 |
| Product code | MOL |
| Recalling firm | Reckitt Benckiser LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 26, 2021 |
| 510(k) numbers | K072169 |
| FEI number | 3011015568 |
At a glance
- 1–9 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