FDA Drug Recalls

105 recalls · Class I, newest first

Sep 27, 2011 Class I · High risk

Labeling: Label Mix up; product labeled did not indicated Extended Release

Terminated Labeling / mix-up Shamrock Medical Solutions Group LLC NDC 53746-178-01 D-1448-2014

Sep 27, 2011 Class I · High risk

Labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL actually contained OxyCODONE HCl 20 mg/mL

Terminated Labeling / mix-up Shamrock Medical Solutions Group LLC NDC 00527-1426-36 D-1447-2014

Sep 27, 2011 Class I · High risk

Labeling: Label Mix Up; packages labeled as Thiamine actually contain Diltiazem Capsules

Terminated Labeling / mix-up Shamrock Medical Solutions Group LLC NDC 62037-0696-90 D-1446-2014

Nov 10, 2010 Class I · High risk

Labeling: Label mix-up; Bottles labeled to contain Morphine Sulfate IR may contain Morphine Sulfate ER and vice-versa.

Terminated Labeling / mix-up Physicians Total Care, Inc NDC 54868-4973-00 D-1386-2012

Nov 10, 2010 Class I · High risk

Labeling: Label mix-up; Bottles labeled to contain Morphine Sulfate IR may contain Morphine Sulfate ER and vice-versa.

Terminated Labeling / mix-up Physicians Total Care, Inc NDC 54868-4033-00 D-1385-2012

Recalls by year