FoodFeb 12, 2020
Tres Coronas Bakery Flour Tortillas are packaged in clear plastic bags, 12 count recall — FDA F-0642-2020
undeclared wheat.
Class IIFDA: TerminatedTres Coronas Bakery
February 2020 recalls — page 20
These records include useful source details for the selected month.
FoodFeb 12, 2020
Lipari Foods Operating Company, LLC Premo Turkey, Bacon, & Cheddar Ciabatta Sandwich, 6 oz. recall — FDA F-0668-2020
Products recalled due to potential contamination with Listeria monocytogenes
Class IFDA: TerminatedLipari Foods Operating Company, LLC.
FoodFeb 12, 2020
Catsmo brand Red Beet recall — FDA F-0579-2020
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedCATSMO LLC
FoodFeb 12, 2020
Almark Foods PECKISH PERFECTLY BOILED FREE RANGE ORGANIC Egg Rancheros recall — FDA F-0622-2020
The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness…
Class IFDA: TerminatedAlmark Foods, LLC
FoodFeb 12, 2020
Lipari Foods Operating Company, LLC Fresh Grab Smoked Turkey Sandwich, 6 oz., UPC recall — FDA F-0665-2020
Products recalled due to potential contamination with Listeria monocytogenes
Class IFDA: TerminatedLipari Foods Operating Company, LLC.
FoodFeb 12, 2020
Lipari Foods Operating Company, LLC Premo and Fresh Grab Asiago Italian Sub Sandwich, 6 oz. recall — FDA F-0652-2020
Products recalled due to potential contamination with Listeria monocytogenes
Class IFDA: TerminatedLipari Foods Operating Company, LLC.
FoodFeb 12, 2020
Almark Foods Eggland's Best Hard Cooked Eggs recall — FDA F-0611-2020
The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness…
Class IFDA: TerminatedAlmark Foods, LLC
FoodFeb 12, 2020
Merical Meijer Joint Health Triple Strength Formula Glucosamine recall — FDA F-0631-2020
Product label does not contain Crustacean Shellfish on the ingredient list or allergen information
Class IIFDA: TerminatedMerical, LLC
FoodFeb 12, 2020
Bakkavor Foods USA TRADER JOE'S OLD FASHIONED Potato Salad NET WT recall — FDA F-0639-2020
The firm was notified by their supplier of boiled eggs that the eggs my be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedBakkavor Foods USA Inc.
FoodFeb 12, 2020
Lipari Foods Operating Company, LLC Premo and Fresh Grab Tuna Salad Wedge Sandwich, 5 oz. recall — FDA F-0657-2020
Products recalled due to potential contamination with Listeria monocytogenes
Class IFDA: TerminatedLipari Foods Operating Company, LLC.
FoodFeb 12, 2020
Almark Foods Fresh Thyme, Giant Eagle, Kroger, Lucerne, Members Mark recall — FDA F-0608-2020
The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness…
Class IFDA: TerminatedAlmark Foods, LLC
FoodFeb 12, 2020
Lipari Foods Operating Company, LLC Premo and Fresh Grab Chicken Salad Wedge Sandwich, 5 recall — FDA F-0656-2020
Products recalled due to potential contamination with Listeria monocytogenes
Class IFDA: TerminatedLipari Foods Operating Company, LLC.
FoodFeb 12, 2020
CATSMO Daniel Boulud brand Baja flavored recall — FDA F-0581-2020
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedCATSMO LLC
FoodFeb 12, 2020
Rachael's brand and Big Y brand Protein Snack Packs recall — FDA F-0597-2020
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedRachael's Food Corporation
DrugFeb 12, 2020
Pioglitazone and Metformin Hydrochloride Tablets, USP 15 mg/500 mg recall — FDA D-0838-2020
Subpotent Drug: Out of specification assay result, below specification, for two lots of Pioglitazone And Metformin Hydrochloride Tablets.
Class IIIFDA: TerminatedMacleods Pharma Usa Inc.
DrugFeb 12, 2020
Teva Pharmaceuticals USA Desmopressin Acetate Tablets, 0.2 mg, 100-count bottle recall — FDA D-0831-2020
GMP Deviations: Product bottle may be absent of desiccant.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugFeb 12, 2020
Minocycline Hydrochloride Extended-Release Tablets, USP, 105 mg*, 30-count bottle recall — FDA D-0827-2020
Failed Dissolution Specifications: low out of specification results for dissolution testing.
Class IIIFDA: TerminatedAscend Laboratories LLC
DrugFeb 12, 2020
PD-Rx Pharmaceuticals ranitidine hydrochloride, USP ,150 mg tablets a) 14-count bottles recall — FDA D-0826-2020
CGMP Deviations: Received notice from supplier of potential -Nitrosodimethylamine (NDMA) amounts above established levels.
Class IIFDA: TerminatedPD-Rx Pharmaceuticals, Inc.
DrugFeb 12, 2020
Graviti Pharmaceuticals Private Atorvastatin Calcium Tablets, USP, 10 mg*, 90-count bottle recall — FDA D-0832-2020
Presence of Foreign Tablets/Capsules: Customer complaint that one 20 mg Atorvastatin Calcium Tablet was present in a bottle labeled as and containing eight-nine Atorvastatin Calcium…
Class IIFDA: TerminatedGraviti Pharmaceuticals Private Limited
DrugFeb 12, 2020
Teva Pharmaceuticals USA Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle recall — FDA D-0830-2020
GMP Deviations: Product bottle may be absent of desiccant.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugFeb 12, 2020
Spectrum Laboratory Products Ranitidine Hydrochloride (powder), USP recall — FDA D-0825-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: TerminatedSpectrum Laboratory Products
DrugFeb 12, 2020
Clonidine Hydrochloride Tablets, USP 0.1mg recall — FDA D-0829-2020
Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to potential migration of Benzophenone at very low level into product from container…
Class IIIFDA: TerminatedUNICHEM PHARMACEUTICALS USA Inc.
DrugFeb 12, 2020
Olmesartan Medoxomil Tablets 20 mg recall — FDA D-0828-2020
cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error with alternate API source prior to filing and approval of Prior Approval Supplement.
Class IIFDA: TerminatedAscend Laboratories LLC
VehicleFeb 6, 2020
Odyssey wiring recall — NHTSA campaign 20V066000
Honda (American Honda Motor Co.) is recalling certain 2018-2020 Odyssey vehicles. The wire harness for the third row seat accessory power outlet may get pinched between the unibody and rear…
wiringHonda (American Honda Motor Co.)
How to use this monthly recall archive
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.