International safety notice
Argon Medical
United Kingdom / MHRA · GBR · Oct 4, 2021
Key facts
| Title | Argon Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | SuperCore Semi-Automatic Biopsy Instrument |
| Manufacturer | Argon Medical |
| Models | 11373084, 11374998, 701218200, 11384243, 11375664, 701116090, 11388461, 701218090, 11376074, 11379722, 11366253, 11365788 and 87 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Oct 4, 2021 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 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