Device recall
Z-0742-2012: New Label: EtchMaster ***Cordless Handpiece***P/N 797 www.GromanDental.com…
FDA device recall · Class III · Groman Inc.
Key facts
| Recall number (Z-number) | Z-0742-2012 |
|---|---|
| Recall event | 58889 |
| Product | New Label: EtchMaster ***Cordless Handpiece***P/N 797 www.GromanDental.com 1800-906-9298 HAZARD WARNING: Using CO2 cartridges from other suppliers may cause an operational hazard and will void the warrantee. Old Label: EtchMaster***Cordless Handpiece***Pats. Pend. Groman, Inc. Adapater P/N 747… |
| Product code | KOJ |
| Recalling firm | Groman Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 17, 2012 |
| FEI number | 3004361444 |
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