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.
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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
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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
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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
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
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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
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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
Ongoing
Historical recordClass II
Snyder's-Lance Inc.
- Product
- Emerald brand Glazed Walnuts; Net WT. 6.5 OZ; Re-sealable po…
- Reason
- Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to the presence of undeclared peanuts, almonds, cashews, and pecans.
- Published
- March 14, 2018
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Vitalab Co Inc
- Product
- Product packaged in the following ways A) Sonne's, No. 17, N…
- Reason
- The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
- Published
- March 14, 2018
- Distribution
- Product distributed to consumers, distri…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
King of Pops
- Product
- Key Lime Pie Handcrafted All-Natural Pop; Net Wt. 3.2 OZ (90…
- Reason
- Undeclared soy allergen
- Published
- March 14, 2018
- Distribution
- GA (distributor) Firm-owned retail f…
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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