Drug recall
Zimmer Dermatone AN, Model No. 88710100
FDA recall event 80466 · Class II · Zimmer Surgical Inc
Key facts
| Event ID | 80466 |
|---|---|
| Recall numbers | Z-2602-2018 |
| Recalling firm | Zimmer Surgical Inc |
| Product type | Devices |
| Products | Zimmer Dermatone AN, Model No. 88710100 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Devices may have a loose control bar, which could compromise the ability to control the thickness of the graft. Devices could also have a loose width plate that if undetected, could result in an… |
| Initiation date | Jun 8, 2018 |
| Report date | Aug 8, 2018 |
| Termination date | Jul 19, 2019 |
| City | Dover |
| State | OH |
| Country | United States |
| FEI number | 1526350 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: