Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.
This recall is currently active, issued April 19, 2024. It was issued by Parker Laboratories, Inc..
- Company
- Parker Laboratories, Inc.
- Recall Initiated
- March 22, 2024
- Posted
- April 19, 2024
- Recall Number
- Z-1604-2024
- Quantity
- 217 cases (1,085 Inner Boxes; 10,850 Eaches)
- Firm Location
- Fairfield, NJ
- Official Source
- View on FDA website ↗
Reason for Recall
Product demonstrates low viscosity.
Distribution
Worldwide distribution - US Nationwide in the states of CA, CO, FL, GA, IL, MD, MI, MN, NC, NE, NY, OH, PA, SC, & TX. The countries of AU, CA, OM, & SA.
Lot / Code Info
Product No. 66-04; UDI: 20855683006399 (Master), 10855683006392 (Inner Box), 00855683006395 (Each); Lot No. (Expiration Date): A1122010 (11/29/25) and A0523002 (5/12/26).
Root Cause
Process change control
Action Taken
An URGENT MEDICAL DEVICE RECALL notification, dated 3/19/24, was emailed to consignees notifying them of this recall. Consignees were asked to examine their inventory for affected devices, quarantine devices identified as part of this recall and discontinue use, and return the email acknowledgement and Recall Stock Response Form to the firm. If product was further distributed, consignees are to conduct their own sub-recalls of affected devices. Consignees with any questions can contact Parker Laboratories by email at ParkerQA@parkerlabs.com or by phone at 973-276-9500x7107 from Monday through Thursday, from 8:30 AM to 5:00 PM, or Friday from 8:30 AM to 1:00 PM.