Device recall
Z-1885-2011: MDI(R), S.A.L.T. Airway Device, Supraglottic Airway Laryngopharyngeal Tube…
FDA device recall · Class II · Microtek Medical Inc
Key facts
| Recall number (Z-number) | Z-1885-2011 |
|---|---|
| Recall event | 57743 |
| Product | MDI(R), S.A.L.T. Airway Device, Supraglottic Airway Laryngopharyngeal Tube, Intended for use with 6.5mm -9.00mm ET tubes, Including SALT(TM) airway, ET tube clamp, Latex-free securing strap, Tongue blade, Lubricating jelly, NON STERILE, REF 79-580, Microtek Medical, Inc., Columbus, MS 39702… |
| Product code | CAE |
| Recalling firm | Microtek Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 20, 2011 |
| FEI number | 1043582 |
At a glance
- None 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