FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MySyrup Sugar Free Madagascar Vanilla Syrup. Product is pack…
- Reason
- Acidified product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MySyrup Sugar Free Hazelnut Syrup. Product is packaged in th…
- Reason
- Acidified product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MySyrup Sugar Free Coconut Syrup. Product is packaged in the…
- Reason
- Acidified product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MySyrup Sugar Free Caramel Syrup. Product is packaged in the…
- Reason
- Acidified product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MySyrup Sugar Free Almond Syrup. Product is packaged in the…
- Reason
- Acidified product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MyChai Chai Tea Concentrate Original Double. Product is pack…
- Reason
- Acidified Chai Tea product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MyChai Chai Tea Concentrate Super. Product is packaged in th…
- Reason
- Acidified Chai Tea product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
My Chai Inc
- Product
- MyChai Chai Tea Concentrate Double. Product is packaged in t…
- Reason
- Acidified Chai Tea product is recalled due to lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
My Chai Inc
- Product
- MyChai Chai Tea Concentrate KALI, 68 fl. oz. Product is pack…
- Reason
- Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
My Chai Inc
- Product
- MyChai Chai Tea Concentrate Original. Product is packaged in…
- Reason
- Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Completed
Historical recordClass II
Hammond's Candies Since 1920 II, LLC
- Product
- Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged…
- Reason
- Undeclared allergen: milk
- Published
- November 13, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Cinacalcet Tablets, 90 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-442-10, b) 90 Tablets per bottle, NDC: 16729-442-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA.
by ACCORD HEALTHCARE, INC.
- Reason
- CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Published
- November 6, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Cinacalcet Tablets, 60 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-441-10, b) 90 Tablets per bottle, NDC: 16729-441-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA.
by ACCORD HEALTHCARE, INC.
- Reason
- CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Published
- November 6, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Cinacalcet Tablets 30 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-440-10, b) 90 Tablets per bottle, NDC: 16729-440-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA.
by ACCORD HEALTHCARE, INC.
- Reason
- CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Published
- November 6, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Cinacalcet Tablets, 90 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India., NDC 43598-369-30.
by Dr. Reddy's Laboratories, Inc.
- Reason
- CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
- Published
- November 6, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Cinacalcet Tablets, 60 mg, 30-count bottles, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India, NDC 43598-368-30.
by Dr. Reddy's Laboratories, Inc.
- Reason
- CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
- Published
- November 6, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Cinacalcet Tablets, 30 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India, NDC 43598-367-30.
by Dr. Reddy's Laboratories, Inc.
- Reason
- CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
- Published
- November 6, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Dakota Tom's, Inc
- Product
- The Gambler, Dakota Toms brand, Net Wt 7.8 oz, individual pr…
- Reason
- Potential Listeria monocytogenes contamination
- Published
- November 6, 2024
- Distribution
- U.S. distribution within states in retai…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Dakota Tom's, Inc
- Product
- Bacon Cheeseburger , Dakota Toms brand, Net Wt 5.7 oz, indiv…
- Reason
- Potential Listeria monocytogenes contamination
- Published
- November 6, 2024
- Distribution
- U.S. distribution within states in retai…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Dakota Tom's, Inc
- Product
- Pepperjack Cheese Burger, Dakota Toms brand, Net Wt 5.7 oz,…
- Reason
- Potential Listeria monocytogenes contamination
- Published
- November 6, 2024
- Distribution
- U.S. distribution within states in retai…
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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