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
Latest records
Latest recalls — page 1470
The newest recall records with useful source details are listed here.
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.
DrugApr 4, 2018
Apollo Care Vancomycin 1.25g added to 250 mL of 0.9% Sodium Chloride IV bag recall — FDA D-0615-2018
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
Akorn 24-HOUR Oral Care q2 Kit with Ballard* Technology, containing 2 Toothbrush Packs with recall — FDA D-0612-2018
Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Class IIIFDA: TerminatedAkorn, Inc.
DrugApr 4, 2018
Renaissance Lakewood Flucanazole Injection, USP 200 mg in in 100 mL (2 mg/mL), 10 Single recall — FDA D-0605-2018
Superpotent and Failed Stability Specifications; out of specification results for assay and water vapor permeability
Class IIIFDA: TerminatedRenaissance Lakewood, LLC
Medical DeviceMar 28, 2018
Arrow International Pressure Injectable Multi- Lumen CVC Kit recall — FDA Z-1165-2018
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best…
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceMar 28, 2018
Arrow International Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with recall — FDA Z-1162-2018
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best…
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceMar 28, 2018
Arrow International Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with recall — FDA Z-1163-2018
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best…
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceMar 28, 2018
Iridex TruFocus LIO Premiere" Laser Indirect Ophthalmoscope ( LIO ) The LIO is a headmounted recall — FDA Z-1075-2018
It was discovered that the laser energy was not going where intended to put it, resulting in focal cataracts and iris burns.
Class IIFDA: TerminatedIridex Corporation
Medical DeviceMar 28, 2018
Arrow International Pressure Injectable Two- Lumen Central Venous Catheterization Kit with recall — FDA Z-1164-2018
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best…
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceMar 28, 2018
Arrow International Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with recall — FDA Z-1161-2018
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best…
Class IIFDA: TerminatedArrow International Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026244 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories