FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Chocolate Bars Birthday Cake UPC 75503858867
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Chocolate Bars Cinnamon Bar UPC 755003858836
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Chocolate Bars Cookie Butter UPC 75500385875…
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Chocolate Bars Cookies & Cream UPC 755003858…
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Infused Cones Strawberry Cheesecake UPC 8101…
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Infused Cones Mint Chocolate Chip UPC 810133…
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Infused Cones Sprinkles UPC 810133320063
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Infused Cones Double Chocolate Chip UPC 8101…
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prophet Premium Blends, LLC
- Product
- Diamond Shruumz Infused Cones Cookies and Cream UPC 81013332…
- Reason
- Toxic levels of muscimol
- Published
- August 7, 2024
- Distribution
- U.S. distribution to the following: AK,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Natural Organics, Inc.
- Product
- NaturesPlus T-MALE Liquid Testosterone Support for Men 8 OZ…
- Reason
- Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
- Published
- August 7, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Natural Organics, Inc.
- Product
- NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost…
- Reason
- Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
- Published
- August 7, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington Homeopathic Products, Inc., Berkley Springs, WV 25411, UPC 7 40640 64300 6.
by Washington Homeopathic Products, Inc.
- Reason
- Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
- Published
- July 31, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Venlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg, packaged in a) 90-count bottles (NDC 68382-034-16) and b)1000-count bottles (NDC 68382-034-10), Rx only, Mfg. by: Zydus Lifesciences Ltd. Ahmedabad, India; Dist. by: Zydus Pharmaceuticals (USA) Inc. Pennington, NJ 08534
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
- Published
- July 31, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass III
Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC Code: 8-40078-56612-7
by GLOBAL WIDGET LLC
- Reason
- Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Published
- July 31, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass III
Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC code: 8-40078-56497-0
by GLOBAL WIDGET LLC
- Reason
- Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Published
- July 31, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass III
Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5
by GLOBAL WIDGET LLC
- Reason
- Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Published
- July 31, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass III
Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, NDC 73423-003-01; UPC Code: 8-40078-56493-2
by GLOBAL WIDGET LLC
- Reason
- Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Published
- July 31, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Pravastatin Sodium Tablets, USP 80mg, packaged in a) 90-count bottle, NDC 68462-198-90; b) 500-count bottle, NDC 68462-198-05, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430,
by Glenmark Pharmaceuticals Inc., USA
- Reason
- Failed Dissolution Specifications: results below specifications
- Published
- July 24, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister card, Rx only, MFG: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-1203-03
by RemedyRePack Inc.
- Reason
- CGMP Deviations: Out of specification for dissolution
- Published
- July 24, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
STELLALIFE ADVANCED FORMULA Peppermint, VEGA Oral Care, Rinse, 16 fl oz (473 ml), Distributed by: StellaLife, 2875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-143-16
by Homeocare Laboratories, Inc.
- Reason
- Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
- Published
- July 24, 2024
- 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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