Device recall
Z-1317-2022: Palindrome H Chronic Catheter, Sterile, Single Use, Rx Only. For acute and…
FDA device recall · Class I · Covidien Llc
Key facts
| Recall number (Z-number) | Z-1317-2022 |
|---|---|
| Recall event | 90311 |
| Product | Palindrome H Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion. |
| Product code | MSD |
| Recalling firm | Covidien Llc |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K112477 |
| FEI number | 1282497 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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