Device recall
Z-0218-2009: Gebauer's Fluro-Ethyl Nonflammable Topical Anesthetic Skin Refrigerant (Aerosol…
FDA device recall · Class II · Gebauer Company
Key facts
| Recall number (Z-number) | Z-0218-2009 |
|---|---|
| Recall event | 49463 |
| Product | Gebauer's Fluro-Ethyl Nonflammable Topical Anesthetic Skin Refrigerant (Aerosol Can) P/N 0386-0020-20. The product consists of a can, a valve and an actuator. Gebauer's Fluro-Ethyl is a vapocoolant (skin refrigerant), topical anesthetic intended to control the pain associated with minor surgical… |
| Product code | MLY |
| Recalling firm | Gebauer Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2010 |
| 510(k) numbers | K002596 |
| FEI number | 1519179 |
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