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Samantha Lynn recalls
FDA enforcement reports naming Samantha Lynn, Inc as the recalling firm.
Recall reports
1
Class I (serious)
1
Most recent report
Dec 5, 2012
All
1
Food
0
Drugs
1
Severity
All classes
Class I: serious
Class II: moderate
Class III: low
Date
Product
Reason
Class
Dec 5, 2012
Reumofan Plus Tablets, 30-count bottle per Box, (remaining label information in Spanish)
Drug ยท Samantha Lynn, Inc
Marketed without an approved NDA/ANDA: Samantha Lynn Inc. is recalling Reumofan Plus Tablets because it contains undeclared drug ingredients making it an unapproved drug.
Class I
