Device recall
Z-0195-2023: Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer…
FDA device recall · Class II · Avanos Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0195-2023 |
|---|---|
| Recall event | 90964 |
| Product | Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: SUMMIT MEDICAL PRODUCTS, REF 220227; MPS Acacia CAT NO: BC-006-04; MEDICAL PRODUCTS SPECIALISTS EXTENSION SET, Catalog Number BC00604, pain control pump accessory |
| Product code | FPA |
| Recalling firm | Avanos Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 31, 2023 |
| FEI number | 3011270181 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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