Device recall
Z-2642-2023: Henke-Ject-2 part luer sterile single use syringes - used for intravenous…
FDA device recall · Class II · Wolf, Henke Sass, Gmbh
Key facts
| Recall number (Z-number) | Z-2642-2023 |
|---|---|
| Recall event | 92836 |
| Product | Henke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneous, intracutaneous and intraarterial injection of liquids or diluted drugs in combination with an adequate medical device or for withdrawal of fluids from the body. Ref: 4100.000V0 |
| Product code | FMF |
| Recalling firm | Wolf, Henke Sass, Gmbh |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K821537 |
| FEI number | 3002807224 |
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