FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Danisco USA Inc.
- Product
- Grindsted WCS 1265 Stabilizer and Emulsifier System, 22.68 k…
- Reason
- Potential Salmonella Contamination
- Published
- June 12, 2024
- Distribution
- US: AZ, CA, CO, FL, IA, ID, IL, IN, KS,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Danisco USA Inc.
- Product
- Grindsted SSD 6018 Stabilizer System, 22.68 kg / 50 lb bag
- Reason
- Potential Salmonella Contamination
- Published
- June 12, 2024
- Distribution
- US: AZ, CA, CO, FL, IA, ID, IL, IN, KS,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Danisco USA Inc.
- Product
- Grindsted Whipped Cream #2 rBST-fr, Stabilizer and Emulsifie…
- Reason
- Potential Salmonella Contamination
- Published
- June 12, 2024
- Distribution
- US: AZ, CA, CO, FL, IA, ID, IL, IN, KS,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Danisco USA Inc.
- Product
- Germantown Stabilizer 1772-II, Stabilizer and Emulsifier Sys…
- Reason
- Potential Salmonella Contamination
- Published
- June 12, 2024
- Distribution
- US: AZ, CA, CO, FL, IA, ID, IL, IN, KS,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Charles Boggini Company Llc
- Product
- Charles Boggini Company Yellow Lemonade and Yellow Lemonade…
- Reason
- Products contain undeclared FD&C Yellow No. 5
- Published
- June 12, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Charles Boggini Company Llc
- Product
- Charles Boggini Company Cola Flavoring Base; packaged in 1 g…
- Reason
- Products contain undeclared sulfites.
- Published
- June 12, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Charles Boggini Company Llc
- Product
- Charles Boggini Pink Lemonde; 1 or 5 U.S. Gallons
- Reason
- Products contain undeclared FD&C Red No. 40
- Published
- June 12, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
Terminated
Historical recordClass II
EYLEA, (aflibercept) Injection, For Intravitreal injection, 2 mg (0.05mL of a 40mg/mL solution), Single-dose Pre-filled Glass Syringe, Rx only, Manufactured by: Regeneron Pharmaceuticals, Inc., 777 Old Saw Mill River Road, Tarrytown, NY 10591, NDC 61755-005-01, NDC (sample lot) 61755-005-54
by Regeneron Pharmaceuticals Inc
- Reason
- Lack of Assurance of Sterility: Complaints of syringe breakage
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), SPF 40+, Broad Spectrum Protective Gel, Sport Performance, NET WT 4 OZ (113g), Manufactured for AGS Brands. UPC 0 17971 10421 7
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%)Enriched with Capsaicin, Aloe Vera, Willow Bark & MSM, Roll-On NET WT 3 fl. oz. (88.7ml), Manufactured for Golden Tiger USA Albuquerque, NM, UPC 1 82294 00006 2
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Roll-On 3 fl oz (88.7ml), painwizard.com Made in the USA, PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00010 9
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%)Enriched with Capsaicin, Aloe Vera, Willow Bark & MSM, Tube 4 oz (113.39 g), Mfr. for Golden Tiger USA Albuq, NM, UPC 1 82294 00002 4
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%)Enriched with Pump Capsaicin, Aloe Vera, Willow Bark & MSM, Bottle with Pump NET WT 32 fl. oz (946.33ml), Manufactured for Golden Tiger LLC Made in USA, UPC 1 82294 00004 8
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 4oz (113.39g), painwizard.com Made in the USA, PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00019 2
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 8 oz (226.79g), Made in the USA, painwizard.com PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00011 6
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), Original Formula, SPF 40+, Broad Spectrum Protective Gel, Sport Performance, NET WT 1 OZ (28 g), Manufactured for AGS Brands.
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion with Water Armor Tech, Broad Spectrum Sunscreen with UVA/UVB Protection, NEW WT. 5 FL OZ (148ML), Distributed by: Bullfrog Brands LLC, PO Box 600207, Dallas, TX 75360 USA. UPC 8 50016 52112 5
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%) Enriched with Capsaicin, Aloe Vera, Willow Bark & MSM, Gallon Jug 128 fl. oz. (3776 ml), Manufactured for Golden Tiger LLC, Made in USA, UPC 1 82294 00005 5
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3
by ARG Laboratories, Inc.
- Reason
- Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Published
- June 5, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free 1mL Single-Use vial for Intraocular Injection, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-640-01
by Imprimis NJOF, LLC
- Reason
- Lack of Assurance of Sterility
- Published
- June 5, 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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