REDUX ELECTROLYTE CREMERecalls & reported problems
Parker Laboratories Inc · Redux Electrolyte Crème, 4 oz. Tube · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Mar 22, 2024Open, Classified
Product demonstrates low viscosity.
Z-1604-2024 · Root cause: Process change control · FDA record ↗
Other Media, Electroconductive devices
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- Ten20 Conductive Paste 10-20-8D. O. Weaver And Company · Media, Electroconductive2 reports
- Nu Skin Conductive Gel 1003913Nse Products, Inc. · MEDIA, ELECTROCONDUCTIVE2 reports
- 3M™ 2345N3m Company · MEDIA, ELECTROCONDUCTIVE1 death1 report
- 3M™ 2346N3m Company · MEDIA, ELECTROCONDUCTIVE1 death1 report
- SIGNAGEL ELECTRODE GELParker Laboratories Inc · Media, Electroconductive1 report
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 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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