FDA Recall United States Terminated Historical recordClass I
GRANDE PRODUCE LTD CO
- Product
- Caribena yellow maradol papaya packed in 35 pound cases
- Reason
- Product is contaminated with Salmonella
- Published
- September 6, 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.
37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,799
Class I recallsReasonable probability of serious health consequences24,349
Class II recallsTemporary or medically reversible health consequences2,891
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
2,072 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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)
- 1,527 recalls have been announced year to date.
- Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
- The highest complete period was Jun 2026 (297).
- Sep 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 | 24,349 |
| Class I | 9,799 |
| Class III | 2,891 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,349 |
| Class I | 9,799 |
| Class III | 2,891 |
| Not Yet Classified | 1 |
FDA Recall Terminated Historical recordClass II
Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, ?Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59
- Reason
- Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47
- Reason
- Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09
- Reason
- Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150. NDC: 0536-1001-85
- Reason
- Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85
- Reason
- Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Phentermine Capsules, 15 mg, a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count bottle (NDC 55289-791-21), d) 30-count bottle (NDC 55289-791-30), e) 60-count bottle (NDC 55289-791-60), Packaged by PD-Rx Pharmaceuticals, Incorporated, Oklahoma City, OK. 73127 Mfg: KVK-Tech, Inc. Newtown, PA 18940
- Reason
- Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10
- Reason
- Labeling: Label Mixup; potentially mislabeled
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Amitriptyline HCL Tablets, USP 50 mg, 100 count bottles, Rx Only, Manufactured for: Qualitest Pharmaceuticals Huntsville, AL 35811, Distributed by: Truxton, Inc. Bellmawr, NJ 08031, NDC: 0463-6352-10
- Reason
- Labeling: Label Mixup; potentially mislabeled
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031
- Reason
- Labeling: Label Mixup; potentially mislabeled
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenobarbital Tablets USP, 60 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6151-10
- Reason
- Labeling: Label Mixup; potentially mislabeled
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6145-10
- Reason
- Labeling: Label Mixup; potentially mislabeled
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10
- Reason
- Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets
- Published
- August 30, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Mary's Harvest Fresh Foods, Inc.
- Product
- Mary's Harvest, Veggie Cup, 6/12 oz pacakges, UPC 0 925047…
- Reason
- Product is recalled due to potential contamination with E.coli O26.
- Published
- August 30, 2017
- Distribution
- distributed in OR and WA
FDA Recall United States Terminated Historical recordClass II
Mary's Harvest Fresh Foods, Inc.
- Product
- Fred Mayer /Garden Highway, VEGETABLE WEEKENDER Kit, Net…
- Reason
- Product is recalled due to potential contamination with E.coli O26.
- Published
- August 30, 2017
- Distribution
- distributed in OR and WA
FDA Recall United States Terminated Historical recordClass II
Mary's Harvest Fresh Foods, Inc.
- Product
- Whole Foods Market, Vegetable Bowl with Hummus, 2/34 oz. pa…
- Reason
- Product is recalled due to potential contamination with E.coli O26.
- Published
- August 30, 2017
- Distribution
- distributed in OR and WA
FDA Recall United States Terminated Historical recordClass II
Mary's Harvest Fresh Foods, Inc.
- Product
- Mary's Harvest, VEGETABLE BLEND NSM, 4/5 lb. packages, no UP…
- Reason
- Product is recalled due to potential contamination with E.coli O26.
- Published
- August 30, 2017
- Distribution
- distributed in OR and WA
FDA Recall United States Terminated Historical recordClass II
Mary's Harvest Fresh Foods, Inc.
- Product
- Kroger QFC, Tandoori Grain & Vegetable Salad, net wt. 10 oz,…
- Reason
- Product is recalled due to potential contamination with E.coli O26.
- Published
- August 30, 2017
- Distribution
- distributed in OR and WA
FDA Recall United States Terminated Historical recordClass II
Mary's Harvest Fresh Foods, Inc.
- Product
- Mary's Harvest, STIR FRY VEGETABLES STORE PACK, net wt. 5 l…
- Reason
- Product is recalled due to potential contamination with E.coli O26.
- Published
- August 30, 2017
- Distribution
- distributed in OR and WA
FDA Recall United States Terminated Historical recordClass II
Mary's Harvest Fresh Foods, Inc.
- Product
- Safeway, Stir Fry Vegetables SW, 4/9.5 oz packages, UPC 8 26…
- Reason
- Product is recalled due to potential contamination with E.coli O26.
- Published
- August 30, 2017
- Distribution
- distributed in OR and WA
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.
