FoodApr 25, 2018
Midwest Northern Nut Pecans Roasted & Salted recall — FDA F-1045-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
April 2018 recalls — page 7
These records include useful source details for the selected month.
FoodApr 25, 2018
Smucker Natural Foods SANTA CRUZ organic BLACKBERRY POMEGRANATE fruit spread NET WT recall — FDA F-1101-2018
The firm was notified that the product did not have an ingredient panel or firm information on the label.
Class IIIFDA: TerminatedSmucker Natural Foods, Inc.
FoodApr 25, 2018
Mrs Gerry's Kitchen Mrs recall — FDA F-1022-2018
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
Midwest Northern Nut Asian Snack Mix recall — FDA F-1049-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
FoodApr 25, 2018
Midwest Northern Net wt recall — FDA F-1071-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
FoodApr 25, 2018
Midwest Northern Trail Mix recall — FDA F-1093-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
FoodApr 25, 2018
Midwest Northern Nut Buffalo Style Peanuts recall — FDA F-1040-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
FoodApr 25, 2018
Midwest Northern Nut Cajun Peanuts recall — FDA F-1039-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
FoodApr 25, 2018
Midwest Northern Roasted NO Salt recall — FDA F-1087-2018
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Class IIFDA: TerminatedMidwest Northern Inc.
FoodApr 25, 2018
Midwest Northern Net Wt recall — FDA F-1072-2018
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 Potato Salad packaged in the following branded and sized recall — FDA F-1029-2018
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 Festival Foods Potato Salad packaged in the following size recall — FDA F-1030-2018
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
Divinity Product Distribution Kratom capsules labeled in the following ways: 1) Divinity recall — FDA F-1020-2018
The firm's dietary supplement products contain kratom (Mitragyna speciosa), a new dietary ingredient for which there is inadequate information to provide reasonable assurance that such…
Class IIFDA: TerminatedDivinity Product Distribution LLC
FoodApr 25, 2018
Seacrest Foods International Formagere de la Brie brand, l' Explorateur, soft ripened recall — FDA F-1116-2018
The cheese has the potential to be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedSeacrest Foods International, Inc.
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.
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
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.