Recall Z-1604-2024— Parker Laboratories, Inc.
Class II · Ongoing
Class II FDA medical device recall by Parker Laboratories, Inc., initiated 2024-03-22. FDA's recall record names no specific 510(k) clearance for this event. Product: Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.. Reason: Product demonstrates low viscosity..
- Recalling firm
- Parker Laboratories, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-03-22
- Firm location
- Fairfield, NJ, United States
Product description
Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.
Reason for recall
Product demonstrates low viscosity.
Data sourced from openFDA. This site is unofficial and independent of the FDA.