FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- WOMAN ORGANIC DARK CHOCOLATE BERRY bar NET WT. 1.8 OZ (51g)…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- TRIM ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.8 OZ (51g) M…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- TRIM ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Manuf…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- RUN ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ (45g) Ma…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- RUN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Manufa…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- MAN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.8 OZ (51g) Manufa…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- HEAL ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Manuf…
- Reason
- The product test positive for almond allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- GOLF ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ (45g) M…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- GOLF ORGANIC CHOCOLATE ALMONDS bar NET WT. 1.6 OZ (45g) Manu…
- Reason
- The product test positive for peanut allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- FOCUS FOR KIDS! SUNFLOWER SEED CHOCOLATE STRAWBERRY bar NET…
- Reason
- The product test positive for peanuts and almond allergen which is not declared on the product label.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- FOCUS ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Manu…
- Reason
- The firm was notified by the State of TN that the product contained undeclared almonds.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8…
- Reason
- The firm was notified by the State of TN that the product contained undeclared almonds.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
eBars
- Product
- DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manu…
- Reason
- The firm was notified by the State of TN that the product contained undeclared peanuts.
- Published
- May 23, 2018
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
Terminated
Historical recordClass I
Ampicillin and Sulbactam for Injection, USP, 3 gram*s/vial, For Intramuscular or Intravenous Use, Sterile, Manufactured for: AuroMedics Pharma LLC, 6 Wheeling Road, Dayton, NJ, NDC 55150-117-20.
by AuroMedics Pharma LLC
- Reason
- Presence of Particulate Matter: confirmed customer report of the presence of visible particulate matter believed to be red rubber particles from the manufacturing process of the active ingredients.
- Published
- May 16, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Minivelle (estradiol transdermal system) 0.0375 mg/day, 1 System per pouch (NDC 68968-6637-1), packaged in 8 pouches per box (NDC 68968-6637-8), Rx only, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186; Dist. by: Noven Therapeutics, LLC, Miami, Florida 33186.
by Noven Pharmaceuticals, Inc.
- Reason
- Defective Delivery System: no longer meets the specification for shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience patches that do not stick well to the skin.
- Published
- May 16, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Minivelle (estradiol transdermal system) 0.1 mg/day, 1 System per pouch (NDC 68968-6610-1), packaged in 8 pouches per box (NDC 68968-6610-8), Rx only, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186; Dist. by: Noven Therapeutics, LLC, Miami, Florida 33186.
by Noven Pharmaceuticals, Inc.
- Reason
- Defective Delivery System: no longer meets the specification for shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience patches that do not stick well to the skin.
- Published
- May 16, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited Bachupally-500 090 India\ NDC 55111-468-01
by Dr. Reddy's Laboratories, Inc.
- Reason
- Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.
- Published
- May 16, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Badger Botanicals LLC
- Product
- Acadica Kratom: Green Hulu 2 Kratom, 250g bags
- Reason
- Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
- Published
- May 16, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Badger Botanicals LLC
- Product
- Acadica Kratom: Red Hulu 2, 250g bags
- Reason
- Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
- Published
- May 16, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Badger Botanicals LLC
- Product
- Acadica Kratom: Green Suma, 250g bags
- Reason
- Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
- Published
- May 16, 2018
- 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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