FDA Recall United States Terminated Historical recordClass I
Vulto Creamery
- Product
- artisanal cheese VULTO Creamery HANDMADE CHEESE, Blue Blais
- Reason
- Listeria monocytogenes contamination
- Published
- April 12, 2017
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,841
Class I recallsReasonable probability of serious health consequences24,366
Class II recallsTemporary or medically reversible health consequences2,892
Class III recallsNot likely to cause adverse health consequencesQuick insights
A snapshot of the most notable patterns across all recorded FDA and USDA recalls.
Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
53 recalls
Most common hazardLack of assurance of sterility
2,073 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026
Download matching recalls as CSV
CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.
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A chart of recalls grouped by month.
Download CSVSummary (Year to date)
- 1,714 recalls have been announced year to date.
- Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
- The highest complete period was Jun 2026 (297).
- Oct 2026 is incomplete and not included in the figures above.
- Complete data
- Incomplete
A bar chart of the total number of recalls in this dataset by recall class.
| Class | Recalls |
|---|---|
| Class II | 24,366 |
| Class I | 9,841 |
| Class III | 2,892 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,366 |
| Class I | 9,841 |
| Class III | 2,892 |
| Not Yet Classified | 2 |
FDA Recall United States Terminated Historical recordClass I
Vulto Creamery
- Product
- artisanal cheese VULTO Creamery HANDMADE CHEESE, ANDES, NET…
- Reason
- Listeria monocytogenes contamination
- Published
- April 12, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Vulto Creamery
- Product
- artisanal cheese VULTO Creamery HANDMADE CHEESE, Willowemoc,…
- Reason
- Listeria monocytogenes contamination
- Published
- April 12, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Vulto Creamery
- Product
- artisanal cheese VULTO Creamery HANDMADE CHEESE, heinennelli…
- Reason
- Listeria monocytogenes contamination
- Published
- April 12, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Vulto Creamery
- Product
- artisanal cheese VULTO Creamery HANDMADE CHEESE, Miranda, NE…
- Reason
- Listeria monocytogenes contamination
- Published
- April 12, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Vulto Creamery
- Product
- artisanal cheese VULTO Creamery HANDMADE CHEESE, Ouleout, NE…
- Reason
- Listeria monocytogenes contamination
- Published
- April 12, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Thortons Italian & Provolone 12 oz.
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Thortons Italian Footlong 6/12 oz.
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Coffee House Italian Flatbread , Item # 226323 net wt. 6 oz…
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Premo Signature Classic Italian, 1/6 oz.
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Premo Italian Wrap, 1/5 oz.
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Premo Asiago Italian Item # 207919, Net Wt 6 oz; Fresh Gr…
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Premo Ham & Provolone Item # 207851, Net Wt 6 oz; Fresh Gr…
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Premo Turkey & Garlic Mayo Item # 207455, Net wt. 5.5 oz; C…
- Reason
- JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
FDA Recall Terminated Historical recordClass III
Montelukast sodium tablets, 10 mg, 30-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: HETERO Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, NDC 31722-726-30
- Reason
- Discoloration: the firm received a complaint of a sealed bottle in which tablets inside had blue spots and a blue powder inside the bottle.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Metronidazole Injection, USP, 500 mg/100 mL, Rx only, Manufactured for: Claris Lifesciences Inc. North Brunswick NJ, 08902, By: Claris Injectable Ltd. Gujarat, India, NDC 36000-001-24
- Reason
- Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ciprofloxacin in Dextrose (5%) Injection, USP, 400 mg in 200 mL 5% Dextrose, Rx only, Manufactured for: Claris Lifesciences Inc. North Brunswick NJ, 08902, By: Claris Injectable Ltd. Gujarat, India, NDC 36000-009-24
- Reason
- Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Sensodyne Repair & Protect Whitening, (stannous fluoride 0.45% (0.15% w/v fluoride ion)), Net Wt. 3.4 oz, Distributed by Glaxo SmithKline Consumer Healthcare LP Moon Township PA 15108 --- NDC 0135-0575-01, UPC UPC: 3 10158 84060 2
- Reason
- Presence of Foreign Substance; low concentration of an additional flavoring ingredient, Patchouli oil resulting in complaints of off flavor/scent
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Atorvastatin Calcium Tablets, 10 mg*, 100-count Unit Dose Tablets (10 x 10) per carton, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.., NDC 51079-208-20
- Reason
- Microbial Contamination of Non-Sterile Products: potential of an elevated bioburden with identification of objectionable organisms.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Atorvastatin Calcium Tablets, 80 mg*, packaged in a) 90-count bottles (NDC 0378-3953-09) and b) 500-count bottles (NDC 0378-3953-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
- Reason
- Microbial Contamination of Non-Sterile Products: potential of an elevated bioburden with identification of objectionable organisms.
- Published
- April 5, 2017
- Distribution
- Nationwide
Data last updated:
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. Read the full medical disclaimer.
