FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass II
Dutch-American Foods Inc
- Product
- French Vanilla Cappuccino, CP302140-12, NET WT. 12 LBS
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- 2-Step White Chocolate Mousse, NET WEIGHT: 1 BAG: 35 oz/ 1…
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- 1-Step White Chocolate Mousse, NET WEIGHT: 1 BAG: 35 oz/ 1…
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- Smoky Bacon Blue Cheese, Net Wt. 50 lbs (22.73 kg), Item Num…
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- Creamy Ranch, Net Wt. 50 lbs (22.73 kg), Item Number 1613150…
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- Texas Sheet Cake Icing Base, Kosher Dairy, Net Wt. 10 lbs, P…
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- CCF Butter Popcorn Seasoning, NET Wt. 1000 lbs, Gluten Free
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- Truco Nacho, NET Wt. 50 lbs (22.73kg)
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 12, 2019Historical recordClass I
Dutch-American Foods Inc
- Product
- Natural Ranch Seasoning, NET Wt. 50 lbs (22.73kg)
- Reason
- Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
- Published
- February 1, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
TerminatedTerminated: January 14, 2021Historical recordClass III
HCG (Chorionic Gonadotropin Lyopholized) II, 1000 unit vial, Rx only, Prepared by Town & Country, Compounding & Consultation Services, 106 Prospect St - 1st FL, Ridgewood, NJ 07459
by Town and Country Compounding and Consultation Services, LLC
- Reason
- Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).
- Published
- January 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: September 14, 2017Historical recordClass III
Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.
by Sandoz Inc
- Reason
- Subpotent Drug: out of specification results for assay test.
- Published
- January 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 22, 2017Historical recordClass II
Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only, Manufactured by Perrigo, Yeruham, Israel, Distributed by Perrigo, Allegan, MI --- NDC 45802-736-84, UPC 345802736840
by L. Perrigo Company
- Reason
- Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
- Published
- January 25, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: April 8, 2019Historical recordClass III
Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets), NDC 69646-704-38 (10 ct. Carton of 1gm samples) / NDC 69646-704-01 (Individual 1gm Samples within Carton), Rx Only, Novum Pharma LLC, Chicago, IL 60654
by Novum Pharma, LLC
- Reason
- Subpotent Drug: Out of specification result for pramoxine hydrochloride
- Published
- January 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 1, 2018Historical recordClass III
Pentasa (mesalamine) Controlled-Release Capsules, 250 mg, 240 count bottle, Rx only, Manufactured for Shire US Inc., Lexington, MA --- NDC 54092-189-81
by Shire PLC
- Reason
- Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles labeled to contain 250 mg capsules
- Published
- January 25, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: June 29, 2017Historical recordClass III
Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
by Teva Pharmaceuticals USA
- Reason
- Failed Dissolution Specifications
- Published
- January 25, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 8, 2017Historical recordClass I
High Liner Foods, Inc.
- Product
- FPI Breaded Round Shrimp Tail-On 1001990, 12-8 oz. cartons…
- Reason
- Product contains undeclared milk and eggs
- Published
- January 25, 2017
- Distribution
- The distribution is specifically in the…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 18, 2017Historical recordClass II
Herr Foods, Inc.
- Product
- Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.…
- Reason
- Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient . The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
- Published
- January 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 18, 2017Historical recordClass II
Herr Foods, Inc.
- Product
- Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 o…
- Reason
- Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.625 oz., and 8.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient. The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
- Published
- January 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: September 12, 2017Historical recordClass I
Fresh Express, Inc.
- Product
- Fresh Express Hearts of Romaine salad, 9 oz., clear/labeled…
- Reason
- Undeclared allergens (milk, wheat, fish (anchovy) and egg.
- Published
- January 25, 2017
- Distribution
- One distributor - Lancaster Foods, Jessu…
View recall →
FDA Recall
TerminatedTerminated: March 20, 2019Historical recordClass II
Daytrana (methylphenidate transdermal system) Transdermal Patch, 30 mg over 9 hours (3.3 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5555-3.
by Noven Pharmaceuticals, Inc.
- Reason
- Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
- Published
- January 18, 2017
- 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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