Chang Kwung Products recalls
FDA enforcement reports naming Chang Kwung Products as the recalling firm.
- Recall reports
- 2
- Class I (serious)
- 2
- Most recent report
- Aug 14, 2013
- Aug 14, 2013Lightning ROD capsules, 550 mg/capsule, packaged in 12-count bottles (UPC 6 89076 20297 8)Drug · Chang Kwung ProductsMarketed Without An Approved NDA/ANDA: Lightning Rod capsules are being recalled because FDA analysis found it to contain an undeclared analogue of sildenafil. Sildenafil is the active ingredient in an FDA-approved pro…Class I
- Aug 14, 2013Lightning ROD capsules, 500 mg/capsule, packaged in 3-count bottles (UPC 6 89076 20257 2)Drug · Chang Kwung ProductsMarketed Without An Approved NDA/ANDA: Lightning Rod capsules are being recalled because FDA analysis found it to contain an undeclared analogue of sildenafil. Sildenafil is the active ingredient in an FDA-approved pro…Class I