FDA Recall
🇺🇸 United States
TerminatedTerminated: June 28, 2018Historical recordClass II
Ventura Foods, LLC
- Product
- A&W All American Food Papa Sauce; 8/24 OZ. Pouches; Net Wt 1…
- Reason
- A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
- Published
- January 24, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 28, 2018Historical recordClass II
Ventura Foods, LLC
- Product
- Sysco Imperial Tartar Sauce; Net Contents 1 GAL; Distributed…
- Reason
- A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
- Published
- January 24, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 28, 2018Historical recordClass II
Ventura Foods, LLC
- Product
- Sysco Imperial Glazed Hot Bacon Dressing; Net Contents 1 GAL…
- Reason
- A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
- Published
- January 24, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 28, 2018Historical recordClass II
Ventura Foods, LLC
- Product
- Gordon Choice Honey Mustard Dressing; Net Contents 128 FL OZ…
- Reason
- A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
- Published
- January 24, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 28, 2018Historical recordClass II
Ventura Foods, LLC
- Product
- Gordon Choice Thousand Island Dressing; Net Contents 128 FL…
- Reason
- A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
- Published
- January 24, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 28, 2018Historical recordClass II
Ventura Foods, LLC
- Product
- Classic Gourmet Dressing; Country French; Net Wt 1.5 OZ.; Ve…
- Reason
- A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
- Published
- January 24, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: January 26, 2018Historical recordClass I
H.I.G. Corporation
- Product
- Frozen Tuna Fillet Saku (Restaurant Supply Only); 22 lbs./2…
- Reason
- Customer tested product and found Listeria monocytogenes in frozen tuna fillet saku
- Published
- January 24, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 29, 2018Historical recordClass I
Gel Spice Co, Inc.
- Product
- Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) an…
- Reason
- Gel Spice, Inc. is recalling three beef flavored bouillon cube products because they contain undeclared allergens -- soy and wheat.
- Published
- January 24, 2018
- Distribution
- The product was distributed thru out the…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 29, 2018Historical recordClass I
Gel Spice Co, Inc.
- Product
- Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) an…
- Reason
- Gel Spice, Inc. is recalling three beef flavored bouillon cube products because they contain undeclared allergens -- soy and wheat.
- Published
- January 24, 2018
- Distribution
- The product was distributed thru out the…
View recall →
FDA Recall
TerminatedTerminated: December 4, 2018Historical recordClass II
Docetaxel Injection USP, 20 mg/mL, One-Vial Formulation, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046 INDIA, NDC 43598-611-11
by Dr. Reddy's Laboratories, Inc.
- Reason
- Defective Container: Product complaints received of defect in the seal of the Docetaxel injection vials that the aluminum seal and/or stopper is removed when the cap is flipped off.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 10, 2019Historical recordClass III
Gabapentin Oral Solution, 250 mg/5 mL (50 mg/mL) in a 470 mL amber-colored bottle, Rx Only. Manufactured by: Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701. NDC: 50383-311-47
by Akorn Inc
- Reason
- CGMP Deviations: Inadvertent release of a drug product with unapproved active ingredient manufacturer.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 16, 2019Historical recordClass II
Valsartan Tablets, USP, 160 mg, 90-count bottles, Rx Only, Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd, Xunqiao, Linhai, Zhejiang 317024, China; Distributed by: Solco Healthcare US, LLC, Cranbury, NJ 08512, USA; NDC 43547-369-09.
by Prinston Pharmaceutical Inc
- Reason
- Failed Tablet/Capsule Specifications: confirmed customer complaint of thicker and heavier tablets in bottle.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: October 1, 2018Historical recordClass II
Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0093-5213-01.
by Teva Pharmaceuticals USA
- Reason
- Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during routine stability testing.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 11, 2020Historical recordClass II
7-Keto DHEA 25mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
by KRS Global Biotechnology, Inc
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 11, 2020Historical recordClass II
7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
by KRS Global Biotechnology, Inc
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 11, 2020Historical recordClass II
Vitamin 10 B Lyophilized Vial, For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
by KRS Global Biotechnology, Inc
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 11, 2020Historical recordClass II
Vitamin 9 A/B Lyophilized Vial, For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
by KRS Global Biotechnology, Inc
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 11, 2020Historical recordClass II
Vitamin 9 Lyophilized Vial, For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
by KRS Global Biotechnology, Inc
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 11, 2020Historical recordClass II
Cyclopentolate HCl/ Phenylephrine HCl/ Tropicamide/ Ketorolac 1%/ 10%/ 1%/ 0.5% Ophthalmic Soln, 5 mL Multi Dose Droptainer, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
by KRS Global Biotechnology, Inc
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 11, 2020Historical recordClass II
Cyclopentolate HCl/ Phenylephrine HCl/ Tropicamide/ Ketorolac 1%/ 2.5%/ 1%/ 0.5% Ophthalmic Solution, 3 mL Multi Dose Droptainer, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
by KRS Global Biotechnology, Inc
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
- Published
- January 17, 2018
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
Read the full medical disclaimer.
