Device recall
Z-2320-2024: Non-sterile, single use, disposable gloves intended for medical purposes to be…
FDA device recall · Class II · SVS LLC
Key facts
| Recall number (Z-number) | Z-2320-2024 |
|---|---|
| Recall event | 94769 |
| Product | Non-sterile, single use, disposable gloves intended for medical purposes to be worn on the hands of examiners to prevent contamination between a patient and an examiner. The gloves are nitrile, powder-free, ambidextrous, and blue-colored with a beaded cuff. The range of sizes includes small, medium… |
| Product code | LZC |
| Recalling firm | SVS LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K220825 |
| FEI number | 3007304336 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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