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.
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 131
Records are ordered by the best available source date.
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.
DrugMay 23, 2018
Apotex Piperacillin and Tazobactam for Injection, USP 3.375 gram/vial* 10-count Single Use recall — FDA D-0839-2018
Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency
Class IFDA: TerminatedApotex Inc.
DrugMay 23, 2018
Prescript Pharmaceuticals Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets, USP recall — FDA D-0809-2018
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
Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets, USP, 20-count M-Pak containers recall — FDA D-0806-2018
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.
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.