FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Bulletproof 360 Inc
- Product
- Fudge Brownie Collagen Protein Bar. Each bar is packed in f…
- Reason
- Fudge Brownie Collagen Protein Bar product is recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- July 12, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Unilever United States, Inc.
- Product
- Ben & Jerry's Pint Slices Chocolate Fudge Brownie 3 chocol…
- Reason
- Unilever is voluntarily recalling a limited number of boxes of Ben & Jerry's Chocolate Fudge Brownie Pint Slices due to undeclared peanut.
- Published
- July 12, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Smucker Foods of Canada Co.
- Product
- Golden Temple No. 1 Fine Durum Atta Flour Blend NET WT 20 LB…
- Reason
- The firm was notified by their Co-packer that the product may be contaminated with E. coli.
- Published
- July 12, 2017
- Distribution
- Product was sent to the following states…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Smucker Foods of Canada Co.
- Product
- Flour sold under the following brands: Golden Temple Durum A…
- Reason
- The firm was notified by their Co-packer that the product may be contaminated with E. coli.
- Published
- July 12, 2017
- Distribution
- Product was sent to the following states…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
GoMacro, Inc.
- Product
- go macro THRIVE Caramel Coconut bar, Net Wt 1.4 oz / 40 G, U…
- Reason
- GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
- Published
- July 12, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
GoMacro, Inc.
- Product
- go macro THRIVE Chocolate, Nuts & Sea Salt bar, Net Wt 1.4 o…
- Reason
- GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
- Published
- July 12, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
GoMacro, Inc.
- Product
- go macro MACROBAR, coconut + almond butter + chocolate chips…
- Reason
- GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
- Published
- July 12, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Bolner's Fiesta Products, Inc
- Product
- Chili Pequino 0.25 oz packaged in a clear plastic bag; Produ…
- Reason
- Low levels of peanuts detected
- Published
- July 12, 2017
- Distribution
- US. AR, AZ, CO, GA, ID, KS, LA, MI, MO,…
View recall →
FDA Recall
Terminated
Historical recordClass II
Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2% sterile, 3.5 g tube, RX only, Manufactured by Allergan, Irvine, California, 92612, U.S.A., NDC: 0023-0313-04.
by Allergan Sales, LLC
- Reason
- Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.
- Published
- July 5, 2017
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass III
BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10
by Mckesson Packaging Services
- Reason
- Failed Moisture Limits: Product tested out-of-specification for moisture content.
- Published
- July 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Doxycycline Hyclate USP, active pharmaceutical ingredient, a) 25 g packaged in a 500 cc container (NDC: 58597-8082-4), b) 100 g packaged in 16 oz container (NDC: 58597-8082-6), c) 500 g packaged in a 2500 cc container (NDC: 58597-8082-7) and a 1,000 g packaged in 1 gallon container (NDC: 58597-8082-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327
by American Pharmaceutical Ingredients LLC
- Reason
- Labeling: Not Elsewhere Classified. Manufacturer and product were discovered to be on FDA Import Alert 66-66 for misbranding of active pharmaceutical ingredient.
- Published
- July 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg, 100-count bottles, Distributed by: GlaxoSmithKline Consumer Healthcare, L.P., Moon Twp, PA 15108, UPC 3 0088-1175-47 8.
by Sanofi-Aventis U.S. LLC
- Reason
- Superpotent Drug: high out-of-specification result for magnesium.
- Published
- July 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Progesterone Injection in Olive Oil With Benzyl Alcohol 10%, 50mg/mL, 10mL Multi-Dose Vial, Rx only, Apothecary by Design, 141 Preble Street, Portland, ME.
by Apothecary By Design
- Reason
- Lack of Processing Controls: The metal container closure adheres to the rubber stopper on some of the units of the batch which can impact the integrity of the container closure.
- Published
- July 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Minivelle (estradiol Transdermal System) 0.1 mg per day, pack of 8 systems per carton, Rx only, Dist. by: Noven Therapeutics, LLC. Miami, Florida 33186. NDC: 68968-6610-8
by Noven Pharmaceuticals, Inc.
- Reason
- Defective Delivery System: Out of specification for peel force from the release liner specification during stability testing at 18M 25C/60%RH.
- Published
- July 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Kroger Co
- Product
- Kroger Dessert Cups yellow sponge cakes NET WT 6.5 oz (184g)…
- Reason
- The firm was notified that the product does not list MILK in the allergen Contains statement, although it is listed in the ingredient statement. They were alerted of this error by a consumer who reported a reaction consistent with a Milk allergy.
- Published
- July 5, 2017
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
Terminated
Historical recordClass II
Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc. Eden Prairie, MN 55344
by Vi-Jon, Inc.
- Reason
- Presence of foreign substance: glass particle
- Published
- June 28, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.
by Lucid Pharma LLC
- Reason
- Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
- Published
- June 28, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Star Snacks Co., Llc.
- Product
- Southern Grove Cashew Halves & Pieces with Sea Salt, Net Wei…
- Reason
- The firm received notification from a consumer finding a glass fragment in Southern Grove Cashew Halves, 8.oz. Source of glass is unknown. It is suspected the glass fragments came in with the raw material.
- Published
- June 28, 2017
- Distribution
- ALDI Distribution Centers. 3/6/2017…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Publix Super Markets, Inc.
- Product
- Publix Deli, Artichoke & Spinach dip, 16 oz., plastic clamsh…
- Reason
- Product may contain glass fragments
- Published
- June 28, 2017
- Distribution
- Distributed to the following states: AL,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Genetic Edge Compounds LLC
- Product
- GEC TNT Thermanite 60 Capsules Dietary Supplement in clear p…
- Reason
- Product contains DMAA and Methylsynephrine.
- Published
- June 28, 2017
- Distribution
- Multiple states
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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