FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Earthworks Health
- Product
- Diatomaceous Earth packaged in the following ways: 1) Per…
- Reason
- Product contains elevated levels of lead, arsenic, and chromium: potentially harmful metals.
- Published
- March 20, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Kradjian Importing Co
- Product
- Bulgarian White Brined Sheep's Milk cheese; 5 gallon can…
- Reason
- Leaking and swollen cans
- Published
- March 20, 2019
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Kradjian Importing Co
- Product
- Zarrin Pickled Cucumbers & Cornichons: Net Weight 101.4 oz.…
- Reason
- Leaking and swollen cans
- Published
- March 20, 2019
- Distribution
- Multiple states
View recall →
FDA Recall
Terminated
Historical recordClass II
Tamsulosin Hydrochloride Capsules, USP, 0.4 mg, 500-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, INDIA; Distributed by Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-450-05.
by Ascend Laboratories LLC
- Reason
- Failed Dissolution Specifications: High Out-of-Specification dissolution results were observed during stability testing.
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan), 0.25%, 4 litres/1.1 US Gallon bottles, packaged in 4 x 4 Litres/1.1 US gallons per case, Petra Hygienic Systems, Concord, ON L4K 4RS/ Reno, NV 89511, NDC 42326-550-01, UPC 0 65936 10335 5.
by Petra Hygienic Systems Int Ltd
- Reason
- Does Not Meet Monograph: product contains, triclosan, an ingredient that can no longer be contained in over-the-counter consumer antiseptic/antibacterial wash products.
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
Completed
Historical recordClass II
Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged as 84 Tablets Blister, 3x1 Unit per carton (NDC 60505-4183-3), Rx Only, Manufactured for: Apotex Corp., Weston, FL 33326; Manufactured by: Oman Pharmaceutical Products Co. L.L.C., P.O. Box 1885, Postal Code 111, Seeb.
by Apotex Inc.
- Reason
- Contraceptive Tablets Out of Sequence: Missing or incorrect tablet placement.
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass I
Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
by Todd Holiday dba Sunstone Organics
- Reason
- MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
- Published
- March 13, 2019
- Distribution
- California, Nebraska, Oregon, Washington
View recall →
FDA Recall
Terminated
Historical recordClass I
White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules (UPC 00859667007361), Sunstone Organics Springfield, Oregon 97473 541-972-3327.
by Todd Holiday dba Sunstone Organics
- Reason
- MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
- Published
- March 13, 2019
- Distribution
- California, Nebraska, Oregon, Washington
View recall →
FDA Recall
Terminated
Historical recordClass I
White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC 00859667007330), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
by Todd Holiday dba Sunstone Organics
- Reason
- MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
- Published
- March 13, 2019
- Distribution
- California, Nebraska, Oregon, Washington
View recall →
FDA Recall
Terminated
Historical recordClass I
Maeng Da Kratom, packaged in a) 25 gram powder (UPC 00859667007118), b) 50 gram powder (UPC 00859667007125), c) 100 gram powder (UPC 00859667007132), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
by Todd Holiday dba Sunstone Organics
- Reason
- MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
- Published
- March 13, 2019
- Distribution
- California, Nebraska, Oregon, Washington
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Kingston Pharma LLC
- Product
- DG Baby Gripe Water herbal supplement with organic ginger an…
- Reason
- Presence of an undissolved ingredient, citrus flavonoid.
- Published
- March 13, 2019
- Distribution
- USA: OH, FL, AZ, WI, MI, AL, CO, UT, NY,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Gasco Industrial, Corp.
- Product
- Gasc¿ Tomato Red Food Color, Net Contents: 5 gal (640 fl. oz…
- Reason
- Failure to declare Yellow #6
- Published
- March 13, 2019
- Distribution
- Domestic Consignees Only. No government…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Gasco Industrial, Corp.
- Product
- Gasc¿ Golden Egg Yellow Shade Food Color, Contains: 32 fl. o…
- Reason
- Failure to declare Yellow #5 and potassium sorbate
- Published
- March 13, 2019
- Distribution
- Domestic Consignees Only. No government…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Twenty-First Century Healthcare, Inc
- Product
- Good Neighbor Pharmacy, D 2000 IU, Dietary Supplement, UPC:…
- Reason
- 21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co Q10 200mg 30ct capsules due the product being mislabeled and potentially containing Vit D 2000 IU.
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Twenty-First Century Healthcare, Inc
- Product
- Good Neighbor Pharmacy, Co Q10 200mg Capsule, Dietary Supple…
- Reason
- 21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co Q10 200mg 30ct capsules due the product being mislabeled and potentially containing Vit D 2000 IU.
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Concord Foods, LLC
- Product
- Concord Fresh Success Mild Salsa Seasoning Mix, Packaged in…
- Reason
- Product contains undeclared allergen, milk.
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Meijer
- Product
- Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clea…
- Reason
- Undeclared soy
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
World Waters, LLC dba WTRMLN WTR
- Product
- Watermelon, WTRMLNWTR Cold Pressured, 12fl oz, Watermelon Fl…
- Reason
- Cold Pressed Juice Watermelon WTRMLN WTR Original 12 packs due to the potential presence of soft plastic that may be loosely floating in some of the finished products.
- Published
- March 13, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Schwan's Global Supply Chain, Inc., Specialy Foods Plant
- Product
- Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Co…
- Reason
- Cheese pizza may contain plastic pieces.
- Published
- March 13, 2019
- Distribution
- Multiple states
View recall →
FDA Recall
Terminated
Historical recordClass III
Moxifloxacin Ophthalmic Solution USP, 0.5%, 3 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-422-01.
by Lupin Pharmaceuticals Inc.
- Reason
- Failed Impurities/Degradation Specifications: Expansion of July 2018 and February 2019 recall due to high out-of-specification for impurities.
- Published
- March 6, 2019
- 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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