DrugAug 30, 2023
Parker Laboratories Helix Pain Relieving Cream (Menthol 7.4%) recall — FDA D-1090-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
Recall history in this database
Classification mix: Class II: 5.
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.
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.