Signia CROS Pure Charge&Go AXRecalls & reported problems
Ws Audiology Usa, Inc. · CROS Pure Charge&Go AX Black · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05714880114867), received between Mar 15, 2024 and Mar 15, 2024 — classified as 1 malfunction.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- No Apparent Adverse Event1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 15, 2024No Apparent Adverse Event; No Apparent Adverse Event
IN THIS EVENT, PATIENT WAS TRAVELING AND WOKE UP TO THE SMELL OF SMOKE WHILE SIGNIA PORTABLE CHARGER WAS PLUGGED IN; PHOTOS PROVIDED SHOW THE CABLE HAD MELTED AND DETACHED FROM PLUGGED IN CHARGER. RESULTS OF TECHNICAL INVESTIGATION SHOWED LOCAL HEAT DAMAGE NEAR USB RECEPTACLE (NOTHING WAS OBSERVED THAT WOULD INDICATE FIRE); THE DEVICE ENCLOSURE AND CABLE INSULATION IS WARPED AND DISCOLORED, CONSISTENT WITH EXPOSURE TO HEAT. THE USB CABLE CONNECTOR WAS DETACHED FROM THE USB CABLE AND IS ATTACHED TO THE USB RECEPTACLE, WHICH IS CONSISTENT WITH THE USB CABLE BEING PULLED FROM THE DEVICE WHILE THE USB CABLE CONNECTOR WAS HOT. FINDINGS SUPPORT THE SUSPECTED ROOT-CAUSE THAT A SHORT CIRCUIT DEVELOPED IN THE USB CONNECTOR OR USB RECEPTACLE DUE TO CORROSION, BENT PINS, OR FOREIGN DEBRIS. CORRECTIVE AND PREVENTATIVE ACTIONS HAVE NOW BEEN IMPLEMENTED AND DOCUMENTED IN A CAPA. PREVENTATIVE ACTION WAS TAKEN TO REDUCE THE PORTABLE CHARGER'S MAXIMUM BATTERY CAPACITY FROM 100% TO 80% TO PREVENT EXTENSIVE BATTERY REACTIONS DURING BATTERY SHORT-CIRCUIT. PREVENTIVE MEASURE WAS VERIFIED TO BE EFFECTIVE IN FURTHER REDUCING THE POSSIBILITY AND SUFFICIENT ENERGY TO CAUSE SEVERE MELTING CASES. NO FURTHER
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 18912974 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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