Parker Laboratories, Inc.: Drug Recall
Recall #D-1089-2023 · 08/02/2023
Class II: Risk
Recall Details
- Recall Number
- D-1089-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Parker Laboratories, Inc.
- Status
- Terminated
- Date Initiated
- 08/02/2023
- Location
- Fairfield, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9
Reason for Recall
CGMP Deviations
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
Distribution Pattern
Nationwide within the United States, Singapore, Korea and Hong Kong
Other Recalls by Parker Laboratories, Inc.
- Class II: Risk 08/02/2023
- Class II: Risk 08/02/2023
- Class II: Risk 08/02/2023
- Class II: Risk 08/02/2023
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.