Drug recall
Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery.
FDA recall event 70919 · Class II · The Anspach Effort, Inc.
Key facts
| Event ID | 70919 |
|---|---|
| Recall numbers | Z-1553-2015 |
| Recalling firm | The Anspach Effort, Inc. |
| Product type | Devices |
| Products | Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The potential exists for the Oscillating Saw Attachment to disengage from the Small Battery Drive handpiece. If the attachment disengages from the handpiece intra-operatively, there is a potential for… |
| Initiation date | Mar 24, 2015 |
| Report date | May 6, 2015 |
| Termination date | Dec 14, 2016 |
| 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: