FoodApr 25, 2018
Aspire Food Group USA EXO Cricket Protein Bar Peanut Butter and Jelly recall — FDA F-1112-2018
Products contain undeclared sulfites
Class IFDA: TerminatedAspire Food Group USA 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 157
Records are ordered by the best available source date.
FoodApr 25, 2018
Midwest Northern Nut Mendakota Mix recall — FDA F-1082-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
FoodApr 25, 2018
Mrs Gerry's Kitchen Mrs recall — FDA F-1027-2018
Firm is recalling various Egg Salads and Potato Salads because they may contain undeclared traces of imitation crab meat
Class IIFDA: TerminatedMrs Gerry's Kitchen, Inc.
FoodApr 25, 2018
Mrs Gerry's Kitchen Mrs recall — FDA F-1025-2018
Firm is recalling various Egg Salads and Potato Salads because they may contain undeclared traces of imitation crab meat
Class IIFDA: TerminatedMrs Gerry's Kitchen, Inc.
FoodApr 25, 2018
Kwik Trip Kitchen's Cravings Egg Salad Sandwich on Oat Multigrain Bread recall — FDA F-1110-2018
Kwik Trip is recalling Kitchen's Cravings Premium Egg Salad Sandwich on Oat Multigrain Bread because it may contain undeclared fish and shellfish.
Class IFDA: TerminatedKwik Trip, Inc.
DrugApr 25, 2018
Partell Specialty Pharmacy Biotin Suspension 10mg/mL, 5 mL amber vial recall — FDA D-0636-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Estradiol 25 mg (SD) pellets in amber vial recall — FDA D-0677-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg, 50 mL amber recall — FDA D-0647-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Testosterone 25 mg pellet recall — FDA D-0664-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Vitamin D 50,000 unit/ml, 5 mL amber vial, Injectable Liquid recall — FDA D-0646-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Testosterone 200 mg pellet recall — FDA D-0662-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy MVI-7 recall — FDA D-0656-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Testosterone 100 mg pellet recall — FDA D-0663-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Ascorbic Acid (Tapioca) 500 mg/mL, 50 mL amber vial recall — FDA D-0634-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Estradiol 40 mg (SD) pellets in amber vial recall — FDA D-0679-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy B-complex recall — FDA D-0635-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Estradiol 20 mg (SD) pellets in amber vial recall — FDA D-0676-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Methionine15mg/Inositol 50mg/Choline 100mg recall — FDA D-0641-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Testosterone 37.5 mg pellet recall — FDA D-0665-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Estradiol 15 mg (SD) pellets in amber vial recall — FDA D-0675-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Testosterone 55 mg pellet recall — FDA D-0668-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Estradiol 35 mg (SD) pellets in amber vial recall — FDA D-0678-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy Testosterone/Finasteride 80 mg/8 mg pellet, amber vial recall — FDA D-0682-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
DrugApr 25, 2018
Partell Specialty Pharmacy TM recall — FDA D-0660-2018
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Class IIFDA: TerminatedPartell Specialty Pharmacy
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.