Drug recall
.***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD…
FDA recall event 62326 · Class II · The Anspach Effort, Inc.
Key facts
| Event ID | 62326 |
|---|---|
| Recall numbers | Z-2077-2012 |
| Recalling firm | The Anspach Effort, Inc. |
| Product type | Devices |
| Products | .***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment ***RX Only Product Usage: Cutting and shaping bone including bones of the spine… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Anspach Effort, Inc. Palm Beach Gardens, FL is recalling their Single Use Sterile Bone Cutting Burrs used with XMax, microMax, microMax Plus, eMax, eMax2 and eMax2 Plus High Speed Drill Systems. It is… |
| Initiation date | Sep 19, 2011 |
| Report date | Aug 1, 2012 |
| Termination date | Jul 25, 2013 |
| City | Palm Beach Gardens |
| State | FL |
| Country | United States |
| FEI number | 1045834 |
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: