FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Tropical Nut & Fruit Company
- Product
- Grabeez The Big Cheese SNACK MIX Net Wt. 3.25 oz (92g) Ingre…
- Reason
- Undeclared Almonds & Cashews. The firm was notified by their customers that the product contains a trail mix instead of the cheese mix. The trail mix contains almonds and cashews that are not listed in the ingredient statement.
- Published
- October 23, 2024
- Distribution
- Products distributed to warehouses, reta…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Gorilla Mind LLC
- Product
- Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appeti…
- Reason
- Product was recalled due to the potential for contamination with Salmonella
- Published
- October 23, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Nuts.com
- Product
- S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranf…
- Reason
- Undeclared Allergen, milk - a mix-up between the product description and the ingredient list. Milk Chocolate was listed in the product description but was missing from the ingredient list.
- Published
- October 23, 2024
- Distribution
- The adulterated product was distributed…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Hydration Labs Inc. dba Bevi
- Product
- Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN…
- Reason
- Product is labeled as electrolytes but is actually caffeine
- Published
- October 23, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Walmart Inc
- Product
- Great Value Cherry Mixed Fruit, 4 oz, 4 Count and 12 count p…
- Reason
- FD&C Red No 3 was not declared as an ingredient.
- Published
- October 23, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Walmart Inc
- Product
- Great Value Diced Peaches, Mandarin Segments, & Cherry Mixed…
- Reason
- FD&C Red No 3 was not declared as an ingredient.
- Published
- October 23, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Today's Frozen Desserts, Inc.
- Product
- Premium Grapenut Special, packaged in paper and plastic cont…
- Reason
- Undeclared Yellow 5 & Yellow 6
- Published
- October 23, 2024
- Distribution
- Product is distributed within the state…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Today's Frozen Desserts, Inc.
- Product
- Premium Grapenut, packaged in paper and plastic containers i…
- Reason
- Undeclared Yellow 5 & Yellow 6
- Published
- October 23, 2024
- Distribution
- Product is distributed within the state…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Today's Frozen Desserts, Inc.
- Product
- Premium Pistachio Grapenut, packaged in paper and plastic co…
- Reason
- Undeclared Yellow 5 & Yellow 6
- Published
- October 23, 2024
- Distribution
- Product is distributed within the state…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Today's Frozen Desserts, Inc.
- Product
- Rum Nut Ice Cream, packaged in paper and plastic containers…
- Reason
- Undeclared Yellow 5 & Yellow 6
- Published
- October 23, 2024
- Distribution
- Product is distributed within the state…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Today's Frozen Desserts, Inc.
- Product
- Rum Raisin Ice Cream, packaged in paper and plastic containe…
- Reason
- Undeclared Yellow 5 & Yellow 6
- Published
- October 23, 2024
- Distribution
- Product is distributed within the state…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection, Single-dose vial, Sterile, Manufacturer Advanced Accelerator Applications, 57 E. Willow Street, NJ 07041, Millburn USA. NDC 69488-0010-61
by Advanced Accelerator Applications USA, Inc.
- Reason
- CGMP deviations
- Published
- October 9, 2024
- Distribution
- FL, MA, NJ, NY, PA, and VA
View recall →
FDA Recall
Ongoing
Historical recordClass II
Ryaltris (olopatadine hydrochloride and mometasone fluorate) Nasal Spray, 665 mcg/25 mcg per spray, 240 Metered Sprays/bottle, 29 g net fill weight, Distr. by Hikma Specialty USA Inc., Columbus, OH 43328, hikma, Glenmark Specialty SA. NDC 59467-700-27.
by Glenmark Pharmaceuticals Inc., USA
- Reason
- Defective Delivery System: The dip tube is clogged causing the spray not to work.
- Published
- October 9, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass I
Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, NDC 61958-2901-2
by Gilead Sciences, Inc.
- Reason
- Presence of Particulate Matter: Presence of glass particle.
- Published
- October 9, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass I
Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199
by Supercore Products Group Inc.
- Reason
- Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
- Published
- October 9, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass I
Hard Steel Capsules packaged in 1 count blister packs in boxes of 10, 20 and 30, Manufactured in U.S.A.
by Supercore Products Group Inc.
- Reason
- Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
- Published
- October 9, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass III
Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm Tube, NDC 68462-0455-47; c) 100 gm Tube, NDC 68462-0455-94, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.
by Glenmark Pharmaceuticals Inc., USA
- Reason
- Defective Container: Firm received complaints of broken tube at the seal.
- Published
- October 9, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Atorvastatin Calcium Tablets, USP, 40mg, Rx only, 1000 Tablets per bottle, Manufactured for: Nivagen Pharmaceuticals, Inc. Sacramento, CA 95827, USA, Manufactured by: Umedica Laboratories Pvt Ltd., Vapi Gujarat 396195, India, NDC: 75834-257-01.
by Nivagen Pharmaceuticals Inc
- Reason
- Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400 mg tablet was found in a 1000-count bottle of Atorvastatin Calcium Tablets, USP 40 mg.
- Published
- October 9, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Blue Tape Sriracha
- Product
- Blue Tape Sriracha sauce is refrigerated condiment, packaged…
- Reason
- Acidified product was manufactured by firm without ODA license.
- Published
- October 9, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Ongoing
Historical recordClass II
Inner Waymark LLC
- Product
- Heart of the Earth (HOTE) 100% Pure Ceremonial Cacao Pre-Gro…
- Reason
- Elevated lead level 0.671 ppm in cacao (chocolate)
- Published
- October 9, 2024
- Distribution
- Distributed to CA, FL, IL, KY, MD, ME, M…
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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