Home / Recalls / Parker Laboratories, Inc. / D-1089-2023

D-1089-2023 Class II Terminated

Recalled by Parker Laboratories, Inc. — Fairfield, NJ

Recall Details

Product Type
Drugs
Report Date
August 30, 2023
Initiation Date
August 2, 2023
Termination Date
June 3, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
9

Product Description

Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%), packaged in a) 2 fl oz/60 mL Pump bottles (NDC 30775-040-02) and b)18 fl. oz./550 ml Pump Bottles (NDC 30775-040-18), Parker Laboratories, Inc. 286 Eldridge Road, Fairfield, NJ 07004

Reason for Recall

CGMP Deviations

Distribution Pattern

Nationwide within the United States, Singapore, Korea and Hong Kong

Code Information

Lot #: a) G0323002, Exp. Date 3/1/2025 Lot #: b) G1122001, Exp. Date 11/15/2024

Other recalls by Parker Laboratories, Inc.

  • Z-1604-2024 Class II — Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte crem (March 22, 2024)
  • Z-1204-2024 Class II — Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inne (January 22, 2024)
  • D-1092-2023 Class II — Helix CBD Therapy Cream (Menthol 7.4%), packaged in a) 3 g pouch (NDC 30775-053- (August 2, 2023)
  • D-1090-2023 Class II — Helix Pain Relieving Cream (Menthol 7.4%), packaged in a) 5 gm pouch (NDC 30775- (August 2, 2023)
  • D-1091-2023 Class II — Helix Tri-Active Therapy Cream (Camphor 3.2%, Menthol 7.4%, Methyl salicylate 12 (August 2, 2023)
  • D-1093-2023 Class II — Helix CBD Clinical Cream (Menthol 7.4%), packaged in a)3 gm pouches (NDC30775-05 (August 2, 2023)
  • Z-1777-2018 Class II — Sterile Aquasonic 100 Ultrasound Transmission Gel, 20 grams, Model Number 01-01- (April 13, 2017)
  • Z-0145-2015 Class II — Parker Eclipse Probe Cover, Latex Free, REF 38-01, 10 Eclipse Probe Covers, Size (August 6, 2014)