Device recall
Z-0871-06: Sterile empty vials, 10mL/20mm closure sold 25/case. Label on vial states…
FDA device recall · Class II · Hollister Stier Laboratories LLC
Key facts
| Recall number (Z-number) | Z-0871-06 |
|---|---|
| Recall event | 35212 |
| Product | Sterile empty vials, 10mL/20mm closure sold 25/case. Label on vial states STERILE EMPTY VIAL Hollister-Stier Laboratories LLC Spokane, WA 99207 USA . Labels on case states 25 STERILE EMPTY VIALS 10 mL/20mm Closure CAUTION: For manufacturing, Processing or Repacking Rx only NON-RETURNABLE LOT… |
| Product code | LDH |
| Recalling firm | Hollister Stier Laboratories LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 3, 2007 |
| FEI number | 3010477 |
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