Device recall
Z-1635-2010: Euflexxa (1% sodium hyaluronate). Pre-filled syringe, Rx only, 3 syringes per…
FDA device recall · Class III · Ferring Pharmaceuticals Inc
Key facts
| Recall number (Z-number) | Z-1635-2010 |
|---|---|
| Recall event | 55407 |
| Product | Euflexxa (1% sodium hyaluronate). Pre-filled syringe, Rx only, 3 syringes per carton; Manufactured by Ferring Pharmaceuticals In, Parsippany, NJ 07054; Manufactured by Bio-Technology General (Israel Ltd. Be er Tuvia, Kiryat Malachi 83104 Israel. Indicated for the treatment of pain in osteoarthritis… |
| Product code | MOZ |
| Recalling firm | Ferring Pharmaceuticals Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 27, 2010 |
| PMA numbers | P010029 |
| FEI number | 1000119907 |
At a glance
- None 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