Device recall
Z-1953-2015: Dr. Sheffield's LUBRI GEL 3 oz (85 g) Non sterile over-the-counter personal…
FDA device recall · Class II · Sheffield Pharmaceuticals, LLC
Key facts
| Recall number (Z-number) | Z-1953-2015 |
|---|---|
| Recall event | 71129 |
| Product | Dr. Sheffield's LUBRI GEL 3 oz (85 g) Non sterile over-the-counter personal lubricant. |
| Product code | MMS |
| Recalling firm | Sheffield Pharmaceuticals, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 10, 2016 |
| 510(k) numbers | K073684 |
| FEI number | 1210513 |
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