FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Parmesan cheese packaged in the following configurations:…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Sargento Bevel Shredded Queso Quesadilla Cheese. Pack Size…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Sargento Deep V Shredded Taco Cheese Blend Material #1000248…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Sargento Part #10129 Fancy Shredded Bistro Blends Nacho & T…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Cheddar cheese packaged in the following configurations: 1…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Monterey Jack cheese packaged in the following configuration…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Asiago cheese packaged in the following configurations: 1.…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Swiss cheese packaged in the following configurations: 1.…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 30, 2024Historical recordClass I
Sargento Foods, Inc.
- Product
- Cotija cheese packaged in the following configurations: 1.…
- Reason
- Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 10, 2024Historical recordClass I
Lakeview Farms LLC
- Product
- Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic con…
- Reason
- Potential contamination of Listeria monocytogenes
- Published
- March 6, 2024
- Distribution
- Alabama/Alaska/ Florida/Georgia/Idaho/Mi…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 4, 2024Historical recordClass II
Reser's Fine Foods, Inc.
- Product
- The recalled Reser's Amish Macaroni Salad was packaged in a…
- Reason
- Undeclared Wheat. The recalled Reser's Amish Macaroni Salad was packaged in a plastic container where the top lid is correctly labeled as Reser s Amish Macaroni Salad but the container side label mis-labeled as Reser s Southern Style with Egg Potato Salad. The ingredient statement on the Reser s Southern Style with Egg Potato Salad container side label does not declare wheat.
- Published
- March 6, 2024
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 13, 2024Historical recordClass II
Mutti USA Inc.
- Product
- MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ)…
- Reason
- Internal can lining is detaching from can into product.
- Published
- March 6, 2024
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 29, 2024Historical recordClass III
Ancient Formulas, Inc.
- Product
- Healthprint Vitamin D3 5000 Dietary Supplement, 200 tablets,…
- Reason
- Product is sub-potent for Vitamin D and label contains incorrect percent daily value.
- Published
- March 6, 2024
- Distribution
- FL
View recall →
FDA Recall
OngoingHistorical recordClass II
Clobazam Tablets 10mg, 100-count bottle, Rx Only, Manufactured by: Micro Labs Limited Goa-403 722, India. Manufactured for: Micro Labs USA, Inc. Somerset, NJ 08873. NDC 42571-315-01
by Micro Labs Limited
- Reason
- CGMP Deviations: Out of specification for residual solvents.
- Published
- February 28, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: October 1, 2024Historical recordClass II
CABTREO (clindamycin phosphate, adapalene and benzoyl peroxide) Topical Gel 1.2%/0.15%/3.1%, Not for Oral, Ophthalmic or Intravaginal Use, Rx Only, Net Wt. 50g, Distributed by Bausch Health US, LLC Bridgewater, NJ 08807 USA, Manufactured by: Bausch Health Companies, Inc. Laval Quebec H7L 448, Canada, NDC 0187-0006-25.
by MCKESSON CORPORATION
- Reason
- CGMP Deviations: Product was stored outside labeled storage temperature requirements. Product was exposed to controlled room temperature environment instead of remaining refrigerated.
- Published
- February 28, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
CompletedHistorical recordClass I
TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 3
by Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company
- Reason
- Chemical Contamination; presence of benzene.
- Published
- February 28, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com
by Today The World
- Reason
- Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.
- Published
- February 28, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
SCHWINNNG Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Today the World LLC, Vancouver, WA 98683
by Today The World
- Reason
- Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.
- Published
- February 28, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
Sustain Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by VSD Productions, Inc. Las Vegas, Nevada
by Today The World
- Reason
- Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this drug an unapproved drug.
- Published
- February 28, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
CompletedHistorical recordClass II
Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80 Summit View Lane, Bastian, VA 24314, Original NDC 42023-159-25 Repack NDC 0404-9810-01
by Henry Schein Inc. and Glove Club HSI Gloves Inc.
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
- Published
- February 28, 2024
- 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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