Erlanger, KY, United States
LGM Pharma LLC recalls
2 recalls recorded since 2018, most recently on 18 December 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)0
Terminated or completed2
Class I (FDA)0
Terminated Class II Drugs
- Recall started
- 18 December 2018
- Terminated
- 9 June 2023
- Reason
- CGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.
- Distribution
- Distributed to MS and Spain
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0486-2019
- CIDOFOVIR DIHYDRATE, (Non-Sterile, For Manufacturing Use), 10g, Rx only, ALP PHARM BEIJING CO., LTD, 12-2-620, Jia 69, Fushi Rd., Haidian, Beijing 100049, China. Batch Number JD-BP-37-20150801
Terminated Class II Drugs
- Recall started
- 24 August 2018
- Terminated
- 11 September 2023
- Reason
- CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
- Distribution
- Nationwide in the USA
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0296-2019
- Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1
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.