FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 43 lb. pail WHITE 'N GLOSSY ICING donut icing, MDM # 1020328…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 35 lb. pail VANILLA XTRA SMOOTH BUTTERCREME FROSTING, MDM #…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 18 lb. pail READY ICE FUDGE ICING, MDM # 10202894, Manufactu…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 14 lb. pail PINK DECORATING BUTTERCREME FROSTING, MDM # 1020…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 18 lb. pail SIMPLICIOUS CREAM CHEESE ICING 18#PL, MDM # 1020…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 45 lb. box SAFEWAY CHOCOLATE BUTTERCREME BASE, MDM # 1020186…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 43 lb. pail GLOSSY WHITE ICING (1102507) donut icing, MDM #…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 40 lb. pail GLAZE 'N SHINE donut glaze, MDM # 10198587, Manu…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 30 lb. cases of 480 1.0 oz frozen chocolate chip with mini c…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CSM Bakery Products
- Product
- 30 lb. cases of 480 1.0 oz frozen chocolate chip cookie doug…
- Reason
- Pieces of plastic polymer were introduced into the sugar system.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Honest Stand
- Product
- Hungry Root Dairy free Garlic Parm sauce, Packaged in 9 oz…
- Reason
- Undeclared Allergen: Product contains both cashews and almonds, but only almonds were labeled on the physical product. Both allergens were labeled on the electronic ingredient statement provided to consumers when they purchased the product directly from Hungry Root Inc.'s website.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Green Water, LLC
- Product
- Taspen's Organics Respiratory Tea, sold in 2 oz packages
- Reason
- The products contain Coltsfoot, which is not to be used internally.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Green Water, LLC
- Product
- Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz D…
- Reason
- The products contain Coltsfoot, which is not to be used internally.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Green Water, LLC
- Product
- Taspen's Organics Breathe Easy Herbal Tincture Dietary Suppl…
- Reason
- The products contain Coltsfoot, which is not to be used internally.
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
ABH Nature's Products, Inc.
- Product
- All Dietary Supplement manufactured and distributed by ABH N…
- Reason
- Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP).
- Published
- February 26, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Theraflu Cough Relief, Dextromethorphan HBr and Guaifensin, 6 packets per carton. Distributed by: GSK Consumer Healthcare, Warren, NJ 07059. NDC carton: 0067-6089-01, NDC packet: 0067-6089-03
by GSK Consumer Health, Inc
- Reason
- Labeling: Label Lacks Warning: Product recalled due to absence of a warning statement on the product label, Ask a doctor before use if you have a sodium-restricted diet.
- Published
- February 19, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Major Extra Strength Acetaminophen Tablets, 500 mg Pain Reliever/Fever Reducer, packaged in a) 100-count bottles (NDC 0904-6730-60; UPC 3 09046 73060 6) and b) 1000-count bottles (NDC 0904-6730-80; UPC 3 09046 73080 4) Distributed by Major Pharmaceuticals 17177 N. Laurel Park Drive, Suite 233 Livonia, MI 45162 USA
by Contract Pharmacal Corporation
- Reason
- Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle.
- Published
- February 19, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Leader Extra Strength Acetaminophen Tablets, 500 mg Pain Reliever/Fever Reducer,100-count bottles,Distributed by Cardinal Health, Dublin OHIO 43017 NDC 7000-0036-1, UPC 0 96295 13807 8
by Contract Pharmacal Corporation
- Reason
- Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle.
- Published
- February 19, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Memantine Hydrochloride Extended Release Capsules, 21 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States. Manufactured by: Lupin Limited Pithampur (M.P.)-454 775, INDIA, NDC 68180-248-06
by Lupin Pharmaceuticals Inc.
- Reason
- Failed Dissolution Specifications: Low out of specification results observed in dissolution test at six-month long-term stability study.
- Published
- February 19, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Raloxifene Hydrochloride Tablets, USP, 60 mg, 30 Tablets (3 x 10 blister cards), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC carton: 60687-266-21; NDC Unit Dose: 60687-266-11
by American Health Packaging
- Reason
- Failed Dissolution Specifications: Low out of specification results obtained during stability testing.
- Published
- February 19, 2020
- 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.
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