Lloyd Inc

FDA Regulatory Profile

Lloyd Inc appears in FDA public data with 4 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1394-2012, Class II) was initiated on February 24, 2012.

Summary

Total Recalls
4
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1394-2012Class IILevothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-0February 24, 2012
D-1395-2012Class IIThyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd PharmFebruary 24, 2012
D-1392-2012Class IIThyro-Tab 0.050mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd PhaFebruary 3, 2012
D-1393-2012Class IILevothroid (levothyroxine sodium tablets, USP), 50 mcg., packaged in 100-ct. bottles, RX, NDC 0456-1February 3, 2012