Complete FDA and NHTSA recall records dated in July 2017.
These records include useful source details for the selected month.
Failed impurities/degradation specifications: This product is being recalled due to out of specification results for Clobetasol Related Compound A, a known impurity which is a degradation…
Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial supplier
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
CGMP Deviations: Lack of quality assurance at the API manufacturer.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
The firm was notified that the product does not list MILK in the allergen Contains statement, although it is listed in the ingredient statement. They were alerted of this error by a…
Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments.
Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments.
The firm was notified by a customer that the label does not include Pecans or Tree Nuts in the Allergy contain statement.
Product contains undeclared tree nuts-cashews
Labeling: Not Elsewhere Classified. Manufacturer and product were discovered to be on FDA Import Alert 66-66 for misbranding of active pharmaceutical ingredient.
Defective Delivery System: Out of specification for peel force from the release liner specification during stability testing at 18M 25C/60%RH.
Superpotent Drug: high out-of-specification result for magnesium.
Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the…
Lack of Processing Controls: The metal container closure adheres to the rubber stopper on some of the units of the batch which can impact the integrity of the container closure.
Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.
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.
