Device recall
Z-0820-05: Moi-Stir oral swabsticks, an aid to mouth care and oral hygiene, CONTENTS: 3…
FDA device recall · Class II · Kingswood Laboratories,Inc
Key facts
| Recall number (Z-number) | Z-0820-05 |
|---|---|
| Recall event | 31780 |
| Product | Moi-Stir oral swabsticks, an aid to mouth care and oral hygiene, CONTENTS: 3 fibre-tipped swabsticks premoistened with MOI-STIR mouth moistening solutioon and saliva supplement; Product Nos. 55299-703-03 and 55299-703-25. Distributed by Kingswood Laboratories, Inc., Indianapolis, IN 46256-3316… |
| Product code | LFD |
| Recalling firm | Kingswood Laboratories,Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 30, 2005 |
| 510(k) numbers | K851026 |
| FEI number | 1827505 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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