Drug recall
Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221
FDA recall event 68495 · Class II · Microline Surgical, Inc.
Key facts
| Event ID | 68495 |
|---|---|
| Recall numbers | Z-1986-2014, Z-1987-2014 |
| Recalling firm | Microline Surgical, Inc. |
| Product type | Devices |
| Products | Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221, Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips (Reusable) Ref 3222 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw |
| Initiation date | May 12, 2014 |
| Report date | Jul 9, 2014 |
| Termination date | Aug 13, 2015 |
| City | Beverly |
| State | MA |
| Country | United States |
| FEI number | 1000137656 |
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: