Complete FDA and NHTSA recall records dated in April 2014.
These records include useful source details for the selected month.
NYSDAM Analysis has revealed the presence of undeclared sulfites in Dried Apricots.
Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month stability time point
Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due to a customer complaint trend…
Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due to a customer complaint trend…
Cross Contamination with Other Products: Product contains Promacta (eltrombopag).
Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due to a customer complaint trend…
Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.
Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.
Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two product dates may cause plastic fragments to break loose and cause a potential…
NYSDAM analysis has revealed the presence of undeclared sulfites and undeclared FD&C Yellow #6 in Golden Natural Brand "Fruit Island".
The Grilling Sauce contains undeclared fish (anchovies), a a sub-ingredient in the Worcestershire Sauce ingredient used in making the product.
HP Hood LLC received one complaint of a foreign object in sour cream product with APR 05 14 code. The object was subsequently identified to be part of a metal bolt from a filling machine.
Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two production dates may cause plastic fragments to break loose and cause a potential…
Product was manufactured using chicken that was reported to be spoiled by another government agency.
Canadian Food Inspection Agency tested a random sample of bagged Italian Blend which tested positive for Listeria Monocytogenes.
Voluntary recall was initiated after identifying a number of packages with punctures on the back of the package that led to spoilage (off odors and appearance).
NUTRA Balance Thickened Water Nectar Thick was found by the FDA to contain mold. In addition, Thickened Water Pudding thick was sampled by Nutra Balance Products and it subsequently tested…
Product contains undeclared wheat
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
