Device recall
Z-0367-2017: Greatbatch, Offset Cup Impactor with the following Parts and Catalogue #: Tl0600…
FDA device recall · Class I · Greatbatch Medical
Key facts
| Recall number (Z-number) | Z-0367-2017 |
|---|---|
| Recall event | 75043 |
| Product | Greatbatch, Offset Cup Impactor with the following Parts and Catalogue #: Tl0600 ~ MMP3100CHA04 T10491 MIMP3100CHA04 T12230 M2M1P3100CHA04 T15752 ~MMP3100CHA04 T15949 ~MMP3100CHA04 T17238 MMP3100CHA04 T9954 MMP3100CHA04 T9955 MMP3100CHA04 T8468 MMP3100CHA04 T11506 MMP3100CHA13 T10281 MMP3100CHA04… |
| Product code | HWA |
| Recalling firm | Greatbatch Medical |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 27, 2017 |
| FEI number | 2183787 |
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