Recall Record

Berkeley Springs, WV, United States

Washington Homeopathic Products, Inc. recalls

5 recalls recorded since 2018, most recently on 31 May 2024. None are listed as ongoing. Status and classification are as published by the FDA.

Recalls5
Ongoing (FDA)0
Terminated or completed5
Class I (FDA)0

Terminated Class III Drugs

Recall started
31 May 2024
Terminated
18 September 2024
Reason
Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
Distribution
Nationwide in the USA
Initiated
Voluntary: Firm initiated
Recall number
D-0618-2024

Terminated Class II Drugs

Recall started
13 May 2022
Terminated
25 May 2023
Reason
cGMP deviations
Distribution
Product was distributed USA nationwide.
Initiated
Voluntary: Firm initiated
Recall numbers
D-1140-2022, D-1129-2022, D-1125-2022, D-1141-2022, D-1135-2022, D-1139-2022, D-1138-2022, D-1133-2022, D-1137-2022, D-1130-2022, D-1132-2022, D-1136-2022 and 5 more

Terminated Class II Drugs

Recall started
20 August 2021
Terminated
21 June 2022
Reason
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Distribution
Distributed Nationwide in the USA
Initiated
Voluntary: Firm initiated
Recall numbers
D-0859-2021, D-0892-2021, D-0858-2021, D-0885-2021, D-0868-2021, D-0866-2021, D-0871-2021, D-0886-2021, D-0857-2021, D-0887-2021, D-0869-2021, D-0862-2021 and 27 more

Terminated Class III Drugs

Recall started
18 March 2021
Terminated
13 May 2021
Reason
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Distribution
Product was distributed to MD, CO & TX only
Initiated
Voluntary: Firm initiated
Recall numbers
D-0322-2021, D-0323-2021, D-0321-2021

Terminated Class II Drugs

Recall started
8 November 2019
Terminated
4 January 2023
Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia
Initiated
Voluntary: Firm initiated
Recall numbers
D-0493-2020, D-0503-2020, D-0502-2020, D-0497-2020, D-0500-2020, D-0506-2020, D-0499-2020, D-0496-2020, D-0491-2020, D-0495-2020, D-0498-2020, D-0494-2020 and 4 more

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.