FoodApr 4, 2018
Wegmans Thai Sweet Chili Sauce Cup 1.5 oz recall — FDA F-0968-2018
The product is labeled as Thai Chili Sauce. The product actually contains Spicy Sauce which contains undeclared egg.
Class IFDA: TerminatedWegmans Food Markets, Inc.
Monthly breakdown
2018 recalls by month
Select a month to review the recall records reported during that period.
December 2018285 records · 4 categoriesNovember 2018342 records · 4 categoriesOctober 2018626 records · 4 categoriesSeptember 2018393 records · 4 categoriesAugust 2018569 records · 4 categoriesJuly 2018356 records · 4 categoriesJune 2018402 records · 4 categoriesMay 2018613 records · 4 categoriesApril 2018449 records · 3 categoriesMarch 2018523 records · 3 categoriesFebruary 2018612 records · 3 categoriesJanuary 2018290 records · 3 categories
2018 recalls — page 168
Records are ordered by the best available source date.
FoodApr 4, 2018
Lancaster Fine Foods 1.5 oz recall — FDA F-0972-2018
The firm received a report that 3 cups labeled as Spicy Mayonnaise Sauce was labeled as Thai Sweet Chili Sauce
Class IFDA: TerminatedLancaster Fine Foods Inc.
FoodApr 4, 2018
Wegmans Food Markets 2 Pack, 5 oz recall — FDA F-0969-2018
The product is labeled as Thai Chili Sauce. The product actually contains Spicy Sauce which contains undeclared egg.
Class IFDA: TerminatedWegmans Food Markets, Inc.
FoodApr 4, 2018
Nestle Dreyers Ice Cream Company Dreyer's Slow Churned Vanilla Bean Ice Cream recall — FDA F-0980-2018
Sales Team employee noticed that some cartons of 48-fl oz. cartons of Dreyers Slow Churned Vanilla Bean Ice Cream contain Butter Pecan ice cream an have a Dreyers Slow Churned Butter Pecan…
Class IIFDA: TerminatedNestle Dreyers Ice Cream Company
FoodApr 4, 2018
IDLife non-GMO, gluten-free and nut-free snack bar for children recall — FDA F-0977-2018
IDLife Kids Bar is labeled as nut free. Allergen testing indicated the presence of almonds and coconut.
Class IIFDA: TerminatedIDLife, LLC
FoodApr 4, 2018
GRIFFITH FOODS Product Name Lot Number or ID Roasted Wing Marinade Seasoning recall — FDA F-0964-2018
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Class IIFDA: TerminatedGRIFFITH FOODS
FoodApr 4, 2018
GRIFFITH FOODS Product Name Lot Number or ID Salt & Vinegar Seasoning - 50 LB recall — FDA F-0966-2018
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Class IIFDA: TerminatedGRIFFITH FOODS
FoodApr 4, 2018
Wegmans Food Markets Family Pack, 17 oz recall — FDA F-0970-2018
The product is labeled as Thai Chili Sauce. The product actually contains Spicy Sauce which contains undeclared egg.
Class IFDA: TerminatedWegmans Food Markets, Inc.
FoodApr 4, 2018
Pepsico diet pepsi caffeine free Classic Diet Pepsi Taste, 12 FL OZ recall — FDA F-0983-2018
Primary package is properly labeled with Aspartame containing liquid but the outer wrap states Aspartame Free.
Class IIIFDA: TerminatedPepsico Inc.
FoodApr 4, 2018
J.M.Rosen Cheesecake J.M recall — FDA F-0973-2018
Retail store employee noticed a small rubber object in the cheesecake - the firm is recalling the entire day's production.
Class IIFDA: TerminatedJ.M.Rosen Cheesecake
FoodApr 4, 2018
Newly Weds Foods Bourbon Brown Sugar Rub SE746665, 50# Bags recall — FDA F-0959-2018
Newly Weds Foods, Inc. initiated a voluntary recall of dry blended seasonings for industrial use due to a supplier's recall of yeast because of the presence of salmonella.
Class IIFDA: TerminatedNewly Weds Foods Inc.
FoodApr 4, 2018
GRIFFITH FOODS Product Name Lot Number or ID Au Jus Seasoning Reduced Sodium recall — FDA F-0967-2018
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Class IIFDA: TerminatedGRIFFITH FOODS
FoodApr 4, 2018
GRIFFITH FOODS Product Name Lot Number or ID Fire Roasted Steak Type recall — FDA F-0963-2018
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Class IIFDA: TerminatedGRIFFITH FOODS
FoodApr 4, 2018
GRIFFITH FOODS Product Name Lot Number or ID Whiskey & Cola Type Flavored recall — FDA F-0960-2018
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Class IIFDA: TerminatedGRIFFITH FOODS
FoodApr 4, 2018
Newly Weds Foods Lbs, flv roast dark type, 30 # Boxes recall — FDA F-0956-2018
Newly Weds Foods, Inc. initiated a voluntary recall of dry blended seasonings for industrial use due to a supplier's recall of yeast because of the presence of salmonella.
Class IIFDA: TerminatedNewly Weds Foods Inc.
FoodApr 4, 2018
GRIFFITH FOODS Product Name Lot Number or ID Premix Roasted Chicken 1258969 recall — FDA F-0965-2018
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Class IIFDA: TerminatedGRIFFITH FOODS
FoodApr 4, 2018
Schwartz Brothers Restaurants dba Schwartz Gourmet Cream Cheese Cinnamon Rolls, packaged in recall — FDA F-0984-2018
Gourmet Cream Cheese Cinnamon Roll is recalled due to undeclared egg.
Class IIFDA: TerminatedSchwartz Brothers Restaurants dba Schwartz Brothers…
DrugApr 4, 2018
Apollo Care Vancomycin 1g added to 250mL of 0.9% Sodium Chloride IV bag recall — FDA D-0614-2018
Stability Data Does Not Support Expiry: 90-day beyond use date (BUD) for the affected product is not supported.
Class IIFDA: TerminatedApollo Care
DrugApr 4, 2018
Evamist recall — FDA D-0608-2018
Defective Delivery System: Potential that cracks in the vial neck near the crimp may result in product evaporation and/or leaking and the inability to properly dispense product.
Class IIFDA: TerminatedPaddock Laboratories, LLC.
DrugApr 4, 2018
Jimmy Weber Red Zone Xtreme 3000 Capsules, Dietary Supplement Product, 1 count blister pack recall — FDA D-0625-2018
Marketed without an Approved NDA/ANDA; FDA analysis found this product to contain undeclared Tadalafil, an FDA approved drug for the treatment of erectile dysfunction.
Class IFDA: TerminatedJimmy Weber
DrugApr 4, 2018
Akorn Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cups (NDC 50383-720-15) recall — FDA D-0611-2018
Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Class IIIFDA: TerminatedAkorn, Inc.
DrugApr 4, 2018
Indomethacin Capsules USP, 50 mg, 100-count bottle recall — FDA D-0606-2018
Labeling: Incorrect Instructions: bottles incorrectly labeled with the usual adult dosage of "One or two capsules 2 or 3 times a day." rather than the correct usual adult dosage of "One…
Class IIIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
DrugApr 4, 2018
E-Z-Paste Barium Sulfate Esophageal Cream (60% w/w), 454 g tube recall — FDA D-0609-2018
Failed stability specifications: Out-of-specification (OOS) result for a preservative assay - methylparaben - during stability testing of one lot.
Class IIFDA: TerminatedBracco Diagnostics Inc.
DrugApr 4, 2018
Akorn 24-HOUR Oral Care q4 Kit with Ballard* Technology, containing 2 Toothbrush Packs with recall — FDA D-0613-2018
Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Class IIIFDA: TerminatedAkorn, Inc.
About the 2018 recall archive
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.