FoodMay 23, 2018
eBars FOCUS FOR KIDS! SUNFLOWER SEED CHOCOLATE STRAWBERRY bar NET WT recall — FDA F-1446-2018
The product test positive for peanuts and almond allergen which is not declared on the product label.
Class IFDA: TerminatedeBars
May 2018 recalls — page 7
These records include useful source details for the selected month.
FoodMay 23, 2018
eBars FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8 recall — FDA F-1444-2018
The firm was notified by the State of TN that the product contained undeclared almonds.
Class IFDA: TerminatedeBars
FoodMay 23, 2018
eBars HEAL ORGANIC CHOCOLATE PEANUT bar NET WT recall — FDA F-1449-2018
The product test positive for almond allergen which is not declared on the product label.
Class IFDA: TerminatedeBars
FoodMay 23, 2018
True Taste Seafood Cold Smoked Mackerel recall — FDA F-1483-2018
Products have the potential to be contaminated Clostridium botulinum.
Class IFDA: TerminatedTrue Taste, LLC.
FoodMay 23, 2018
True Taste Seafood Cold Smoked Whitefish recall — FDA F-1487-2018
Products have the potential to be contaminated Clostridium botulinum.
Class IFDA: TerminatedTrue Taste, LLC.
FoodMay 23, 2018
True Taste Seafood Hot Smoked Salmon recall — FDA F-1485-2018
Products have the potential to be contaminated Clostridium botulinum.
Class IFDA: TerminatedTrue Taste, LLC.
FoodMay 23, 2018
eBars RUN ORGANIC CHOCOLATE ALMOND bar NET WT recall — FDA F-1451-2018
The product test positive for peanut allergen which is not declared on the product label.
Class IFDA: TerminatedeBars
FoodMay 23, 2018
True Taste Seafood Hot Smoked Mackerel recall — FDA F-1482-2018
Products have the potential to be contaminated Clostridium botulinum.
Class IFDA: TerminatedTrue Taste, LLC.
FoodMay 23, 2018
eBars FOCUS ORGANIC CHOCOLATE PEANUT bar NET WT recall — FDA F-1445-2018
The firm was notified by the State of TN that the product contained undeclared almonds.
Class IFDA: TerminatedeBars
FoodMay 23, 2018
True Taste Seafood Hot Smoked Whitefish recall — FDA F-1486-2018
Products have the potential to be contaminated Clostridium botulinum.
Class IFDA: TerminatedTrue Taste, LLC.
FoodMay 23, 2018
eBars GOLF ORGANIC CHOCOLATE ALMONDS bar NET WT recall — FDA F-1447-2018
The product test positive for peanut allergen which is not declared on the product label.
Class IFDA: TerminatedeBars
FoodMay 23, 2018
A G Specialty Foods 9 oz recall — FDA F-1442-2018
Coconut is declared in the Ingredients statement but it is not declared in the Contains statement.
Class IIFDA: TerminatedA G Specialty Foods, Inc.
FoodMay 23, 2018
HEALTHY FOOD INGREDIENTS Great Value Organic Ground Flax Seed, Net Wt recall — FDA F-1473-2018
Great Value Organic Ground Flax Seed has the potential to contain metal fragments.
Class IIFDA: TerminatedHEALTHY FOOD INGREDIENTS
FoodMay 23, 2018
eBars DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz recall — FDA F-1443-2018
The firm was notified by the State of TN that the product contained undeclared peanuts.
Class IFDA: TerminatedeBars
DrugMay 23, 2018
Sulfamethoxazole and Trimethoprim Tablets USP, 800 mg/160 mg recall — FDA D-0802-2018
Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of Sulfamethoxazole and Trimethoprim Tablets USP, 800 mg/160 mg (500 ct.) because a foreign matter identified as…
Class IIFDA: TerminatedSun Pharmaceutical Industries, Inc.
DrugMay 23, 2018
Boiron Calendula Cream, calendula officinalis 1X HUS-10%, 2.5 oz. tubes recall — FDA D-0803-2018
Labeling: Labeling Error on Declared Strength; The outer carton (secondary packaging) statement of ingredients misstates the concentration of active ingredient at 7%. The primary packaging…
Class IIIFDA: TerminatedBoiron Inc.
DrugMay 23, 2018
Prescript Pharmaceuticals Clindamycin 300 mg capsules, USP, 28-count M-Pak containers recall — FDA D-0808-2018
Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C…
Class IIFDA: TerminatedPrescript Pharmaceuticals, Inc.
DrugMay 23, 2018
Scopolamine Transdermal Therapeutic System, 1 mg/3 days, a) 4-count (NDC 45802-580-84) recall — FDA D-0816-2018
Defective delivery system
Class IIFDA: TerminatedL. Perrigo Company
DrugMay 23, 2018
Piperacillin and Tazobactam for Injection, USP 3.375 grams per vial, For Intravenous Use recall — FDA D-0926-2018
Presence of Particulate Matter: confirmed customer report for presence of visible particulate matter, confirmed as glass
Class IFDA: TerminatedAuroMedics Pharma LLC
DrugMay 23, 2018
Prescript Pharmaceuticals Clindamycin 150 mg capsules, USP, 30-count M-Pak container recall — FDA D-0805-2018
Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C…
Class IIFDA: TerminatedPrescript Pharmaceuticals, Inc.
DrugMay 23, 2018
Riomet recall — FDA D-0818-2018
Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this recall in response to identified labeling discrepancies in the patient literature.
Class IIIFDA: TerminatedSun Pharmaceutical Industries, Inc.
DrugMay 23, 2018
Prescript Pharmaceuticals Chlorhexidine 0.12% liquid, 473 MILLITERS recall — FDA D-0807-2018
Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C…
Class IIFDA: TerminatedPrescript Pharmaceuticals, Inc.
DrugMay 23, 2018
Mylan Pharmaceuticals Amlodipine and Benazapril HCL Capsules, USP, 5 mg/10 mg, 100 count recall — FDA D-0819-2018
cGMP Deviations; cleaning process for equipment used to manufacture the specified batches was not followed according to procedure
Class IIFDA: TerminatedMylan Pharmaceuticals Inc.
DrugMay 23, 2018
Mylan Pharmaceuticals Amlodipine and Benazapril HCL Capsules, USP, 5 mg/40 mg, 100 count recall — FDA D-0820-2018
cGMP Deviations; cleaning processes for equipment used to manufacture the specified batches was not followed according to procedure
Class IIFDA: TerminatedMylan Pharmaceuticals Inc.
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.