FDA Drug Recalls

Recalls / Class I

Class ID-0486-2024

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

Sapropterin Dihydrochloride Powder for Oral Solution 100mg, 30 individual packets per carton, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-477-30.

Affected lot / code info
Lot # T2200352, Exp. 12/31/2024

Why it was recalled

Sub-potent Drug; powder discoloration associated with decreased potency

Recalling firm

Firm
Dr. Reddy's Laboratories, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
107 College Rd E, N/A, Princeton, New Jersey 08540-6623

Distribution

Quantity
2402 cartons
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2024-04-08
FDA classified
2024-05-06
Posted by FDA
2024-05-15
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0486-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.