Ra Medical Systems, Inc. recalls
Every recall we track for Ra Medical Systems, Inc. — 6 in all, from 2018–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Ra Medical Systems, Inc. peaked in 2020 (3); 6 since 2017.
All FDA recall records for Ra Medical Systems, Inc. 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 | 1 | 1 |
| 2019 | 0 | 1 | 1 | 0 | 2 |
| 2020 | 0 | 3 | 0 | 0 | 3 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 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 Ra Medical Systems, Inc. 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 Ra Medical Systems, Inc. recalls
6 shown- Use cautionMedical device
Ra Medical Systems, Inc. recalls DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in ablating a channel in occlusive peripheral vascular
Ra Medical Systems recalls DABRA RA-308 Excimer Laser units with footswitch that may fail if liquids spill, risking unintended laser activation during vascular procedures.
Ra Medical SystemsOct 16, 2020 - Use cautionMedical device
Ra Medical Systems, Inc. recalls DABRA RA-308 Excimer Laser, SN: ******* - Product Usage: The device is intended for use in ablating a channel in
Ra Medical Systems recalls DABRA RA-308 Excimer Lasers with taller wheel mounting that may fall over, causing injury. Affected units have specific serial numbers listed in the recall.
Ra Medical SystemsJul 24, 2020 - Use cautionMedical device
Ra Medical Systems, Inc. recalls DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and
Ra Medical recalls DABRA Laser (RA-308) systems due to software issues that could cause unintended laser light release, risking user or patient injury. Affected units have serial numbers RA00027 to RA00176.
Ra Medical SystemsJan 23, 2020 - Lower riskMedical device
Ra Medical Systems, Inc. recalls Ra Medical Systems DABRA Catheter 5F (1.5mm), REF: 1222-5000-01, LOT: 18-090400-094, USE BY: 2019-09-24, MFR DATE:
Ra Medical Systems recalls DABRA Catheter 5F (1.5mm) models with potential calibration failures due to shelf life exceeding labeled expiration. Affected units have specific lot numbers and use-by dates.
Ra Medical SystemsSep 19, 2019 - Use cautionMedical device
Ra Medical Systems, Inc. recalls Pharos Excimer Laser, Model: EX-308 - Product Usage: The Pharos EX-308 Excimer Laser System is designed to treat the
Ra Medical Systems recalls EX-30:8 excimer laser systems due to software error causing over-treatment risks. Affected units may cause skin blisters or strong redness. Contact for remedy.
Ra Medical SystemsAug 23, 2019 - UnratedMedical device
Ra Medical Systems Inc recalls The DABRA Laser (model RA-308) is designed to provide ultraviolet laser energy endovascularly through a catheter to
Ra Medical Systems recalls DABRA Laser (model RA-308) due to potential laser calibration errors during setup, which could affect medical procedures. Affected units have specific serial numbers.
Ra Medical SystemsFeb 15, 2018
Ra Medical Systems, Inc. recall questions
How many recalls has Ra Medical Systems, Inc. had?
6 recalls from Ra Medical Systems, Inc. are on record with U.S. safety agencies, from 2018–2020.
What is the most recent Ra Medical Systems, Inc. recall?
Ra Medical Systems, Inc. recalls DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in ablating a channel in occlusive peripheral vascular, dated Oct 16, 2020. Every Ra Medical Systems, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Ra Medical Systems, Inc. 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 Ra Medical Systems, Inc. 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.