Device recall
Z-1278-2015: Puritan absorbent foam tipped applicator; Catalog Number 25-1406 1 PF BT…
FDA device recall · Class II · Puritan Medical Products Co., LLC
Key facts
| Recall number (Z-number) | Z-1278-2015 |
|---|---|
| Recall event | 70270 |
| Product | Puritan absorbent foam tipped applicator; Catalog Number 25-1406 1 PF BT. Sterile absorbent foam tipped applicator used to apply medication or to obtain specimens from a patient. |
| Product code | KXG |
| Recalling firm | Puritan Medical Products Co., LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 18, 2015 |
| FEI number | 1216735 |
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