Device recall
Z-0932-05: Tyco Healthcare Kendall Argyle Neonatal Pediatric PICC, 1.9 Fr/Ch x 30 cm Dual…
FDA device recall · Class II · Kendall Healthcare Products Co
Key facts
| Recall number (Z-number) | Z-0932-05 |
|---|---|
| Recall event | 32022 |
| Product | Tyco Healthcare Kendall Argyle Neonatal Pediatric PICC, 1.9 Fr/Ch x 30 cm Dual Lumen PICC Catheter, REF 43304. A single catheter in a thermoformed tray with a Tyvek lid. The lidded tray is packaged one per carton. Firm on label: Tyco Healthcare, Mansfield, MA. Product sold sterile, 10 units per… |
| Product code | LJS |
| Recalling firm | Kendall Healthcare Products Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 27, 2005 |
| 510(k) numbers | K042461 |
| 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