Simpleware Product Group, SYNOPSYS NORTHERN EUROPE recalls
Every recall we track for Simpleware Product Group, SYNOPSYS NORTHERN EUROPE — 2 in all, all from 2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Simpleware Product Group, SYNOPSYS NORTHERN EUROPE since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Simpleware Product Group, SYNOPSYS NORTHERN EUROPE product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Simpleware Product Group, SYNOPSYS NORTHERN EUROPE recalls
1 shownSimpleware Product Group, SYNOPSYS NORTHERN EUROPE recall questions
How many recalls has Simpleware Product Group, SYNOPSYS NORTHERN EUROPE had?
2 recalls from Simpleware Product Group, SYNOPSYS NORTHERN EUROPE are on record with U.S. safety agencies, from 2021.
What is the most recent Simpleware Product Group, SYNOPSYS NORTHERN EUROPE recall?
Simpleware Product Group, SYNOPSYS NORTHERN EUROPE recalls Simpleware ScanIP software. For transfer of imaging information from a medical scanner to an output file, and for, dated Jun 4, 2021. Every Simpleware Product Group, SYNOPSYS NORTHERN EUROPE recall is listed on this page, newest first.
What should I do if I have a recalled Simpleware Product Group, SYNOPSYS NORTHERN EUROPE product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Simpleware Product Group, SYNOPSYS NORTHERN EUROPE recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.