Device recall
Z-2109-2010: MICROTEK MEDICAL, INC, STACKHOUSE LASER RESISTANT SUCTION PROBE, Size: 1/4" x 9"…
FDA device recall · Class II · Microtek Medical Inc
Key facts
| Recall number (Z-number) | Z-2109-2010 |
|---|---|
| Recall event | 56130 |
| Product | MICROTEK MEDICAL, INC, STACKHOUSE LASER RESISTANT SUCTION PROBE, Size: 1/4" x 9" (0.64cm x 22.9cm), REF 24014, QTY 10 EA, STERILE EO, 2015-05, Microtek Medical, Inc. , Columbus, MS 39702, www.microtekmed.com, CE0044, EC REP Microtek Medical B.V. , Zutphen, The Netherlands, Manufactured in the U.S.A… |
| Product code | FYD |
| Recalling firm | Microtek Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 12, 2010 |
| 510(k) numbers | K001082 |
| FEI number | 1043582 |
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