Device recall
Z-2793-2015: Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100…
FDA device recall · Class II · Ecolab Inc
Key facts
| Recall number (Z-number) | Z-2793-2015 |
|---|---|
| Recall event | 71957 |
| Product | Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100, ORS-110, ORS-130, ORS-300, ORS-301, ORS-320, ORS-321, ORS-325, ORS-330, ORS-331 and ORS-2200. The ORS Fluid Warming and Slush Drapes are individually wrapped and placed in poly-Tyvek pouches with a label insert, then… |
| Product code | LHC |
| Recalling firm | Ecolab Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 9, 2017 |
| 510(k) numbers | K021288, K023282 |
| 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