FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Plant Devas Inc
- Product
- Blemish Face Care Kit; Each kit contains: Tea Tree Gel Cle…
- Reason
- FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
- Published
- March 21, 2018
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Plant Devas Inc
- Product
- Blue Face Care Kit; Each kit contains: Blue Lavender Clean…
- Reason
- FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
- Published
- March 21, 2018
- Distribution
- Nationwide
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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
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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
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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
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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
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
RIPPLE FOODS PBC
- Product
- ripple Chocolate Nutritious Pea Milk; 48 oz. plastic bottle…
- Reason
- Firm recalled product after finding high levels of coliforms, as well as Serratia liquefaciens.
- Published
- March 21, 2018
- Distribution
- Distribution centers in GA, IA, OH.
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
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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
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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
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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
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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
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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
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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
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Lotte International America Corp.
- Product
- Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g…
- Reason
- Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
- Published
- March 14, 2018
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
La Pasta, Inc.
- Product
- HEINEN'S Potato Gnocchi * Preservative Free * 9 oz. (225 g)…
- Reason
- LA PASTA, INC has initiated a recall of Heinen's Potato Gnocchi 9 oz. , because of a undeclared milk allergen .
- Published
- March 14, 2018
- Distribution
- The product was distributed to the follo…
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.
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