Device recall
Z-1635-2013: - Cannulated Drill Bit for Mini TightRope Ref. AR-8911DC Lot 122511 - Drill Bit…
FDA device recall · Class II · Surgical Instrument Service And Savings, Inc.
Key facts
| Recall number (Z-number) | Z-1635-2013 |
|---|---|
| Recall event | 65205 |
| Product | - Cannulated Drill Bit for Mini TightRope Ref. AR-8911DC Lot 122511 - Drill Bit, Straight Shank 2.7mm x 12.7cm Ref. 2318-027-00 Lot 122322 - Drill Bit, w/Depth Mark, Quick Coupling (Red) 2.0mm x 140mm Ref. 323.062 Lot 122347 - Fast Cutting Drill Bit 2.0mm Ref. FDB 2.0 Lot 122289, 122322 - Midas Rex… |
| Product code | HTW |
| Recalling firm | Surgical Instrument Service And Savings, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2013 |
| FEI number | 3002299608 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database