Device recall
Z-2191-2011: Forteo [teriparatide (rDNA origin) injection] black starter kits containing…
FDA device recall · Class II · Eli Lilly and Company
Key facts
| Recall number (Z-number) | Z-2191-2011 |
|---|---|
| Recall event | 58219 |
| Product | Forteo [teriparatide (rDNA origin) injection] black starter kits containing Triad alcohol pads. The starter kits look like insulated lunch boxes and contain alcohols pads, needles, instruction guides, and freezer gel packs. Note: the kits do not contain the drug, Forteo. Intended use: Travel starter… |
| Product code | KMJ |
| Recalling firm | Eli Lilly and Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2011 |
| FEI number | 1819470 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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