FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Plant Devas Inc
- Product
- Rose Face Care Kit; Each kit contains: Rose Cleansing Milk…
- Reason
- FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Plant Devas Inc
- Product
- Green Tea Clay; 2.1 and 0.17 oz. jars evanhealy Han…
- Reason
- FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Plant Devas Inc
- Product
- French Rose Clay; with Mineral Rish Moroccan Rhassoul Clay…
- Reason
- FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Plant Devas Inc
- Product
- Lemongrass Facial Polish with Oats, Fengreek & Neem. 3 oz c…
- Reason
- FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Plant Devas Inc
- Product
- Clay Mask Kit; 2 glass jars of clay: Green Tea Clay 0.3 oz.…
- Reason
- FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Kodiak Cakes, LLC
- Product
- Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 O…
- Reason
- The frozen waffle product contains whey but fails to declare the major food allergen "milk" on the label
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Progressive Laboratories, Inc
- Product
- Xenesta Nuvive Womens 90 count packaged in a white plastic b…
- Reason
- Recalled dietary supplements may contain undeclared milk.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Progressive Laboratories, Inc
- Product
- Xenesta Nuvive Mens 90 count packaged in an white plastic bo…
- Reason
- Recalled dietary supplements may contain undeclared milk.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Progressive Laboratories, Inc
- Product
- Thyroid Resilience 120 count bottle packaged in an amber pla…
- Reason
- Recalled dietary supplements may contain undeclared milk.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Progressive Laboratories, Inc
- Product
- Testosterzone 180 count bottle packaged in an amber plastic…
- Reason
- Recalled dietary supplements may contain undeclared milk.
- Published
- March 21, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10
by Mckesson Packaging Services
- Reason
- Failed Stability Specifications
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
labetalol HCl injection 20 mg/4 mL (5mg/mL), 4 mL syringe, Rx Only, for IV Use, SCA Pharmaceuticals, Windsor, CT 06095 --- NDC 70004-0700-28, UPC 70004070028
by SCA Pharmaceuticals, LLC.
- Reason
- Labeling; Incorrect or Missing Lot number/Expiration Date; some product labels incorrectly indicates a compounding date of 12/27/2018 and use-by date of 03/27/2019 instead of 12/27/2017 and use-by-date of 03/27/2018
- Published
- March 14, 2018
- Distribution
- GA, NE & PA
View recall →
FDA Recall
Terminated
Historical recordClass III
Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP Wilmington, DE 19850 by: Patheon Pharmaceuticals, Inc. Cincinnati OH 45237 Product of Switzerland NDC 0310-0657-58
by AstraZeneca Pharmaceuticals LP
- Reason
- Failed Impurities/Degradation Specifications; elevated levels of quality attribute Form L (polymorph).
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Methylphenidate Hydrochloride Extended-release Tablets, USP, 36 mg, 100-count bottle, Rx only, Trigen Laboratories, LLC Bridgewater, NJ 08807. NDC 13811-708-10
by Osmotica Pharmaceutical Corp
- Reason
- Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER Tablets 36 mg found to contain 1 27 mg Methylphenidate HCL ER Tablet.
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-215-05
by Akorn, Inc.
- Reason
- Failed Stability Specification: OOS low viscosity results discovered during retain testing.
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Labetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx only, labeled as a) Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-20; and b) NOVAPLUS, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-25.
by Hospira Inc. A Pfizer Company
- Reason
- Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Caribbean Red Hot Cheese Packaged i…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Chicken Soup Cheese Packaged in the…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Chipotle Cheese Packaged in the fol…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Cheese Packaged in the following si…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
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.
