FoodNov 8, 2017
America New York Ri Wang Food Group Co Item# 076 - Fish Tofu with Shrimp Filling Net Weight recall — FDA F-0078-2018
Product contains undeclared milk.
Class IFDA: TerminatedAmerica New York Ri Wang Food Group Co. Ltd.
Monthly breakdown
2017 recalls by month
Select a month to review the recall records reported during that period.
December 2017112 records · 2 categoriesNovember 2017262 records · 2 categoriesOctober 201750 records · 2 categoriesSeptember 2017124 records · 2 categoriesAugust 2017178 records · 2 categoriesJuly 2017212 records · 2 categoriesJune 2017121 records · 3 categoriesMay 2017245 records · 3 categoriesApril 2017306 records · 2 categoriesMarch 2017226 records · 2 categoriesFebruary 2017106 records · 2 categoriesJanuary 2017396 records · 2 categories
2017 recalls — page 15
Records are ordered by the best available source date.
FoodNov 8, 2017
Pacific Coast Fruit Company Kit Cauliflower Tabouleh, 2/4.5 lbs., Food Service item # recall — FDA F-0046-2018
Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm…
Class IFDA: TerminatedPacific Coast Fruit Company
FoodNov 8, 2017
Wegmans Food Markets 2 Pack, 6 oz recall — FDA F-0082-2018
Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.
Class IIFDA: TerminatedWegmans Food Markets, Inc.
FoodNov 8, 2017
Triple B Broccoli Crunch Kit, Alaska Carrot brand, 1 x 6 lb recall — FDA F-0161-2018
Broccoli Crunch Kit product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of…
Class IFDA: TerminatedTriple B Corporation
FoodNov 8, 2017
America New York Ri Wang Food Group Co Item #013 - Fried Pollock Balls Net Weight: 227g 8oz recall — FDA F-0073-2018
Product contains undeclared milk.
Class IFDA: TerminatedAmerica New York Ri Wang Food Group Co. Ltd.
FoodNov 8, 2017
Midway Specialty Vehicles Oatmeal Cookie, 60-2.5 oz recall — FDA F-0150-2018
Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain…
Class IIFDA: TerminatedMidway Specialty Vehicles LLC
FoodNov 8, 2017
Albertsons Ready recall — FDA F-0055-2018
Recall of Ready. Chef. Go! Seafood meal bags after notification that they were produced with vegetable products recalled by supplier for potential Listeria monocytogenes.
Class IIFDA: TerminatedAlbertsons Inc.
FoodNov 8, 2017
Pacific Coast Fruit Company Vegetable Tray, 2/25 oz., RETAIL item # 71444, Pacific Coast recall — FDA F-0043-2018
Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm…
Class IFDA: TerminatedPacific Coast Fruit Company
FoodNov 8, 2017
Midway Specialty Vehicles Triple Chocolate Mudslide Cookie, 120 1 oz recall — FDA F-0143-2018
Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain…
Class IIFDA: TerminatedMidway Specialty Vehicles LLC
FoodNov 8, 2017
Triple B Stir Fry Kit, Alaska Carrot, 1 x 11 lb recall — FDA F-0163-2018
Stir Fry Kit product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas,…
Class IFDA: TerminatedTriple B Corporation
DrugNov 8, 2017
Kiriko, LLC A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle recall — FDA D-0058-2018
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine, making this an unapproved drug for…
Class IIFDA: TerminatedKiriko, LLC.
DrugNov 8, 2017
SCA Pharmaceuticals ROCuronium Bromide 10 mg per mL, 5 mL Fill in single dose syringe recall — FDA D-0068-2018
Lack Of Assurance Of Sterility.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugNov 8, 2017
SCA Pharmaceuticals HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in 0.9% Sodium recall — FDA D-0061-2018
Lack Of Assurance Of Sterility.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugNov 8, 2017
Teva Pharmaceuticals USA Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg recall — FDA D-0069-2018
Failed dissolution specifications; all lots within expiry are being recalled due to out of specification dissolution results.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugNov 8, 2017
SCA Pharmaceuticals PHENYLephrine HCl 100 mcg per mL In 0.9% Sodium Chloride 10 mL Fill recall — FDA D-0066-2018
Lack Of Assurance Of Sterility.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugNov 8, 2017
SCA Pharmaceuticals morphine sulfate 1 mg per mL in 0.9% Sodium Chloride a) Total Volume 100 recall — FDA D-0064-2018
Lack Of Assurance Of Sterility.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugNov 8, 2017
SCA Pharmaceuticals HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 recall — FDA D-0060-2018
Lack Of Assurance Of Sterility.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugNov 8, 2017
SCA Pharmaceuticals fentanyl as citrate 2 mcg per mL BUPIvacaine HCl 0.125% recall — FDA D-0062-2018
Lack Of Assurance Of Sterility.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugNov 8, 2017
Precision Dose Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups recall — FDA D-0057-2018
Subpotent Drug: low out of specification results.
Class IIIFDA: TerminatedPrecision Dose Inc.
DrugNov 8, 2017
SCA Pharmaceuticals fentaNYL as citrate 2 mcg / mL, ROPIVacaine HCl 0.1%, Total Fentanyl recall — FDA D-0063-2018
Lack Of Assurance Of Sterility.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugNov 8, 2017
Sanofi-Aventis U.S Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial recall — FDA D-0056-2018
Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.
Class IIIFDA: TerminatedSanofi-Aventis U.S. LLC
DrugNov 8, 2017
AVKARE Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per recall — FDA D-0055-2018
Failed Impurities/Degradation Specifications: slightly elevated levels of phthalic acid.
Class IIFDA: TerminatedAVKARE Inc.
FoodNov 1, 2017
Dr. Pepper Snapple Group Diet Rite, Pure Zero Cola, 0 calories, 0 caffeine, 0 sodium recall — FDA F-0030-2018
Product is labeled to be caffeine-free but contains caffeine.
Class IIFDA: TerminatedDr. Pepper Snapple Group Inc.
FoodNov 1, 2017
Beyond Better Foods ENLIGHTENED THE GOOD-FOR-YOU ICE CREAM 60 CALORIES PER SERVING recall — FDA F-0033-2018
Product contains undeclared coconut.
Class IIFDA: TerminatedBeyond Better Foods LLC
About the 2017 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.