Device recall
Z-0946-2014: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL, featuring IsoSilk(R), 5"…
FDA device recall · Class II · Ecolab Inc
Key facts
| Recall number (Z-number) | Z-0946-2014 |
|---|---|
| Recall event | 65667 |
| Product | MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL, featuring IsoSilk(R), 5" x 98", (13cm x 249 cm), REF 3688, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS 39702 |
| Product code | KKX |
| Recalling firm | Ecolab Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 14, 2014 |
| 510(k) numbers | K882724 |
| FEI number | 1000289767 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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