Medical DeviceMay 1, 2024
Parker Laboratories Redux Electrolyte Creme, Product Ref. 66-04 recall — FDA Z-1604-2024
Product demonstrates low viscosity.
Class IIFDA: OngoingParker Laboratories, Inc.
Recall history in this database
Classification mix: Class II: 8.
Medical DeviceMar 6, 2024
Parker Laboratories Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains recall — FDA Z-1204-2024
Five complaints were received related to viscosity of Tensive Conductive Adhesive Gel Ref 22-60.
Class IIFDA: OngoingParker Laboratories, Inc.
DrugAug 30, 2023
Parker Laboratories Helix Pain Relieving Cream (Menthol 7.4%) recall — FDA D-1090-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
DrugAug 30, 2023
Parker Laboratories Helix Tri-Active Therapy Cream recall — FDA D-1091-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
DrugAug 30, 2023
Parker Laboratories Helix CBD Therapy Cream (Menthol 7.4%) recall — FDA D-1092-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
DrugAug 30, 2023
Parker Laboratories Helix CBD Clinical Cream (Menthol 7.4%) recall — FDA D-1093-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
DrugAug 30, 2023
Parker Laboratories Protex Foaming Hand Sanitizer recall — FDA D-1089-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
Medical DeviceMay 16, 2018
Parker Laboratories Sterile Aquasonic 100 Ultrasound Transmission Gel, 20 grams, Model recall — FDA Z-1777-2018
There is a potential for the gel packets to have leaks in the packet seal.
Class IIFDA: TerminatedParker Laboratories, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Parker Laboratories, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.