Parker Laboratories, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1604-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

Product Classification:

Class II

Date Initiated: March 22, 2024

Date Posted: May 1, 2024

Recall Number: Z-1604-2024

Event ID: 94303

Reason for Recall:

Product demonstrates low viscosity.

Status: Ongoing

Product Quantity: 217 cases (1,085 Inner Boxes; 10,850 Eaches)

Code Information:

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).

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated