International safety notice
DePuy Synthes
United Kingdom / MHRA · GBR · Oct 31, 2019
Key facts
| Title | DePuy Synthes |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | EIT Implants (Cervical, PLIF, TLIF) |
| Manufacturer | DePuy Synthes |
| Models | E14LA00141, E15LA00211, PEI41302, E15LA00901, E15LA00351, E15LA00511, PEI81326, E14LA00391, E15LA01501, E15LA00431, CEI8070S, E15LA00631 and 306 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Oct 31, 2019 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1