Device recall
Z-1219-2007: Biogel Skinsense Polyisoprene Surgical Gloves, Non-Latex, Sterile, (Size 8) Made…
FDA device recall · Class II · Molnlycke Health Care, Inc
Key facts
| Recall number (Z-number) | Z-1219-2007 |
|---|---|
| Recall event | 39362 |
| Product | Biogel Skinsense Polyisoprene Surgical Gloves, Non-Latex, Sterile, (Size 8) Made in Malaysia |
| Recalling firm | Molnlycke Health Care, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 17, 2010 |
| FEI number | 1629080 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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