Xstrahl Limited recalls
Every recall we track for Xstrahl Limited — 3 in all, from 2021–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Xstrahl Limited 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 | 2 | 0 | 0 | 2 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 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 Xstrahl Limited 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 Xstrahl Limited recalls
3 shown- Lower riskMedical device
Xstrahl Limited recalls X80 RADiant Photoelectric Therapy System
Xstrahl recalls X80 RADiant Photoelectric Therapy Systems with specific lot codes due to potential compatibility issues with replacement treatment applicators. Affected units may not function properly with new applicators.
XstrahlApr 27, 2022 - Use cautionMedical device
Xstrahl Limited recalls Treatment applicator for Gulmay Medical 150 or Xstrahl 150 superficial X-ray therapy system
Xstrahl Limited recalls 150-series superficial X-ray therapy systems due to risk of base plate detaching from the main body. Affected models include GM0072 through GM0506. Contact for repair or return.
XstrahlAug 27, 2021 - Use cautionMedical device
Xstrahl Limited recalls Concerto User Interface Software provided with the following systems: (1) Xstrahl 100 Electronic Brachytherapy - 100kV
Xstrahl recalls Concerto software versions V2.0-V2.2 for Xstrahl 100-300 systems. Editing treatment plans with 2 opposing beams before approval can cause mis-treatment errors. Affected users should contact Xstrahl for guidance.
XstrahlApr 26, 2021
Xstrahl Limited recall questions
How many recalls has Xstrahl Limited had?
3 recalls from Xstrahl Limited are on record with U.S. safety agencies, from 2021–2022.
What is the most recent Xstrahl Limited recall?
Xstrahl Limited recalls X80 RADiant Photoelectric Therapy System, dated Apr 27, 2022. Every Xstrahl Limited recall is listed on this page, newest first.
What should I do if I have a recalled Xstrahl Limited 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 Xstrahl Limited 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.