CLINICAL LASERTHERMIA SYSTEMS AB recalls
Every recall we track for CLINICAL LASERTHERMIA SYSTEMS AB — 3 in all, all from 2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from CLINICAL LASERTHERMIA SYSTEMS AB peaked in 2021 (3); 3 since 2017.
All FDA recall records for CLINICAL LASERTHERMIA SYSTEMS AB 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 | 3 | 0 | 3 |
| 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 |
Most common reasons for CLINICAL LASERTHERMIA SYSTEMS AB recalls
What to do if you have a recalled CLINICAL LASERTHERMIA SYSTEMS AB 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 CLINICAL LASERTHERMIA SYSTEMS AB recalls
1 shownCLINICAL LASERTHERMIA SYSTEMS AB recall questions
How many recalls has CLINICAL LASERTHERMIA SYSTEMS AB had?
3 recalls from CLINICAL LASERTHERMIA SYSTEMS AB are on record with U.S. safety agencies, from 2021.
What is the most recent CLINICAL LASERTHERMIA SYSTEMS AB recall?
CLINICAL LASERTHERMIA SYSTEMS AB recalls Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR, dated Apr 1, 2021. Every CLINICAL LASERTHERMIA SYSTEMS AB recall is listed on this page, newest first.
Why are CLINICAL LASERTHERMIA SYSTEMS AB products recalled?
The most common reasons on record: single use devices labeled as sterile may not have been adequately sterilized (3).
What should I do if I have a recalled CLINICAL LASERTHERMIA SYSTEMS AB 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 CLINICAL LASERTHERMIA SYSTEMS AB 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.