Device recall
Z-2035-2024: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product…
FDA device recall · Class III · Avanos Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2035-2024 |
|---|---|
| Recall event | 94518 |
| Product | NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral Syringe Amber NonSterile, Product Code BA-S05EO; b. 12mL Oral Syringe Amber NonSterile, Product Code BA-S12EO; c. 1mL Oral Syringe Amber NonSterile, Product Code BA-S1EO; d. 20mL Oral Syringe Amber… |
| Product code | KYX |
| Recalling firm | Avanos Medical, Inc. |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 3011270181 |
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