FDA Drug Recalls

Recalls / Class I

Class ID-1478-2022

Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.

Product

Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73

Affected lot / code info
Lot# 20076A, EXP Jul. 2022, 20079A, 20081A, EXP Aug. 2022; 21096A, EXP Oct. 2022; 21115A, 21103A, EXP Sep. 2022.

Why it was recalled

Microbial Contamination of Non-Sterile Products.

Recalling firm

Firm
Plastikon Healthcare LLC
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
3780 Greenway Cir, N/A, Lawrence, Kansas 66046-5440

Distribution

Quantity
220,500 cups
Distribution pattern
Distributed Nationwide in the USA

Timeline

Recall initiated
2022-06-07
FDA classified
2022-09-06
Posted by FDA
2022-09-14
Terminated
2025-06-25
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1478-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class I recall: drug · FDA Drug Recalls