Stop using nowMedical device recall · FDA · Published July 17, 2019
Laborie Solar Blue Laptop Power Supply Recall: Fire Hazard Risk
Laborie Medical recalls Solar Blue Urodynamics power supplies due to fire risk from flammability issues. Affected units have specific serial numbers. Stop using immediately to prevent fire.
Power supply unit (PS-SBL) not correctly labeled, and insulation material used at the low voltage DC end does not meet all applicable flammability rating requirements. may lead to a potential fire hazard
Take action
Contact the company
📍Recalling firmLABORIE MEDICAL TECHNOLOGIES, CORP400 Avenue D Ste 10 · Williston, VT 05495-7828
“Laborie Solar Blue Laptop Power Supply Recall: Fire Hazard Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67416-laborie-solar-blue-laptop-power-supply-recall-fire-hazard-risk. Based on FDA recall #Z-2076-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2076-2019%22&limit=1).
Laborie Medical Technologies Corp recalled the U3-3 Solar Blue laptop integrated power supply on July 17, 2019, according to the FDA. The agency said the unit may present a potential fire hazard due to incorrect labeling and insulation material that does not meet flammability requirements.
How to tell if you have it
Brand: Laborie Medical
Product: U3-3 Solar Blue, Laptop integrated power supply used with the Solar Blue Urodynamics
Serial Numbers: PE18-7SBL1452, PE18-7SBL 1414
Units affected: 2
The hazard
The power supply unit (PS-SBL) was not correctly labeled, and the insulation material used at the low voltage DC end does not meet all applicable flammability rating requirements. According to the FDA, this may lead to a potential fire hazard.
Context
GovInfoNow's records show Laborie Medical Technologies Corp has one other recall on record since May 21, 2026: the Solar GI System Recall regarding moisture risk in pneumatic circuits. Other recent recalls of similar products include the Philips Allura Xper FD10C Medical System Recall (Dec. 15, 2025), the Philips Allura Xper FD10F Medical System Recall (Dec. 15, 2025), and the Olympus SOLTIVE Laser System Recall (Feb. 27, 2026).
How to tell if you have this one
Check for serial numbers starting with PE18-7SBL on the power supply. The product is used with Solar Blue Urodynamics for urinary tract assessments.
Brand
Laborie Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Stop Using Immediately
The power supply may cause a fire if used. Do not use the unit until you contact Laborie Medical.
Where it went and when
Where it was distributed
Distributed in Arizona and Pennsylvania.
Listed by the agency
Not listed
FDA distribution: “US distribution in AZ, and PA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Pennsylvania.
Recall timeline
FDA terminated this recall 4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2076-2019 (July 17, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2076-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.