ImprimisRx CA, Inc., dba ImprimisRx Timolol-Brimonidine-Dorzolamide-Latanoprost recall — FDA D-1133-2017
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Complete FDA and NHTSA recall records dated in 2017, organized for browsing by month, category and recalling company.
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Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Labeling: Label mix-up. Finished product Povidone iodine 7.5% was labeled as Povidone iodine 10% , the outer box had the correct label.
Ingredient used in the manufacture of these products was recalled due to a potential for Listeria monocytogenes contamination.
Ingredient used in the manufacture of these products was recalled due to a potential for Listeria monocytogenes contamination.
Recall of crackers due to pieces of blue grade plastic liner found inside the packaged cracker product.
The product has been recalled due to the potential to be contaminated with Listeria monocytogenes.
German Chocolate cakes were labeled as Chocolate Iced Yellow Cake. German Chocolate contains pecans that are not listed on the Iced Yellow Cake label.
Missing ingredient statement on the label and undeclared soy.
According to the firm ( Nuts.com) undeclared cashews were in the Bourbon Street Mix. The firm learned of the problem through a customer complaint. The firm is doing a recall of the product…
Ingredient used in the manufacture of these products was recalled due to a potential for Listeria monocytogenes contamination.
Mislabeled Outer Box labeled as : KIND Breakfast Dark Chocolate Cocoa Bars may contain KIND Breakfast PROTEIN Dark Chocolate Cocoa Bars.
Ingredient used in the manufacture of these products was recalled due to a potential for Listeria monocytogenes contamination.
The recalling firm received papayas from a Mexican grower associated with an outbreak of Salmonella.
Ingredient used in the manufacture of these products was recalled due to a potential for Listeria monocytogenes contamination.
Ingredient used in the manufacture of these products was recalled due to a potential for Listeria monocytogenes contamination.
Crystallization: Particulate matter (Ketorolac Calcium Salt) was observed from several lots of retained samples.
Presence of Foreign Substance: customer complaint of blue foreign material identified as a portion of a nitrile glove was discovered in product.
Defective container: Oral solution leaking from container.
Undeclared yellow # 5
Undeclared allergens: Butter fails to disclose the presence of milk and ice cream sandwiches fail to disclose the presence of wheat.
Product is recalled due to potential contamination with E.coli O26.
The Best Bar Ever initiated a voluntary recall of the Peanut Butter Crunch flavor (40g size) because the individual wrapper mistakenly has a gluten-free logo on the label. The wrapper for…
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.