Shamrock Medical Solutions Group metFORMIN ER Tablets, 500 mg, Rx, Packaged and labeled as recall — FDA D-1448-2014
Labeling: Label Mix up; product labeled did not indicated Extended Release
Overview of recall records associated with Shamrock Medical Solutions Group LLC, including dates, categories and classifications where available.
Classification mix: Class II: 3, Class I: 3.
Labeling: Label Mix up; product labeled did not indicated Extended Release
Labeling: Label Mix up; product labeled to contain Docusate Sodium 240mg instead of Docusate Calcium 240mg
Labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL actually contained OxyCODONE HCl 20 mg/mL
Labeling: Label Mix Up; packages labeled as Thiamine actually contain Diltiazem Capsules
Labeling: Label Mix up; product labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg instead of Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg
Labeling: Label Mix up; product labeled to contain Nebivolol tablets actually contained Pramipexole Dihydrochloride tablets
This page summarizes recall records in which the official source identifies Shamrock Medical Solutions Group LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.