Device recall
Z-2229-2011: Kits and Trays containing alcohol swabstick/prep pad: GEO-MED BIOPSY TRAY, V A…
FDA device recall · Class II · Deroyal Industries, Inc. Lafollette
Key facts
| Recall number (Z-number) | Z-2229-2011 |
|---|---|
| Recall event | 58675 |
| Product | Kits and Trays containing alcohol swabstick/prep pad: GEO-MED BIOPSY TRAY, V A MED CTR MARTINSBURG, REF 89-7617.01 Rx Only, STERILE EO, Distributed by Geo-Med, LLC, 478 Altamonte Drive, Ste. 108, PMB 235, Altamonte Springs, FL 37201; DeRoyal (R) ST TPN/CVC DRG KIT W/VAD, REF 47-003, Rx Only, STERILE… |
| Product code | LRP |
| Recalling firm | Deroyal Industries, Inc. Lafollette |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2014 |
| FEI number | 3005011024 |
At a glance
- None 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