Device recall
Z-0910-04: Medtronic MiniMed Paradigm Quick-set Plus Infusion Sets. Models MMT-359S6…
FDA device recall · Class I · Medtronic MiniMed
Key facts
| Recall number (Z-number) | Z-0910-04 |
|---|---|
| Recall event | 35768 |
| Product | Medtronic MiniMed Paradigm Quick-set Plus Infusion Sets. Models MMT-359S6; MMT-359S9; MMT359L6; & MMT-359L9. (differences in models is variation in length, 6 versus 9mm) |
| Product code | FPA |
| Recalling firm | Medtronic MiniMed |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 19, 2012 |
| 510(k) numbers | K030149 |
| FEI number | 3003166194 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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