Drug recall
Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in…
FDA recall event 65391 · Class II · Advanced Orthogonal Equipment, Incorporated
Key facts
| Event ID | 65391 |
|---|---|
| Recall numbers | Z-1809-2013 |
| Recalling firm | Advanced Orthogonal Equipment, Incorporated |
| Product type | Devices |
| Products | Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unapproved medical device |
| Initiation date | Mar 6, 2013 |
| Report date | Jul 31, 2013 |
| Termination date | Nov 25, 2019 |
| City | Saint Petersburg |
| State | FL |
| Country | United States |
| FEI number | 3006315109 |
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: