FDA Drug Recalls

Recalls / Class I

Class ID-1477-2022

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

MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 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 0904-6840-72.

Affected lot / code info
Lot # 20074A, EXP Jul. 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
7,700 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-1477-2022. 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