FDA Recall United States Terminated Historical recordClass II
EAT REAL FOOD LLC
- Product
- Plant Based Yogurt Culina Blueberry Lavender Nt Wt 5 oz. (14…
- Reason
- Potential for glass to be found in product
- Published
- July 13, 2022
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,113
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,793
Class I recallsReasonable probability of serious health consequences24,343
Class II recallsTemporary or medically reversible health consequences2,887
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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026
Download matching recalls as CSV
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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 | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
FDA Recall United States Terminated Historical recordClass I
Pure Ground Ingredients
- Product
- Pure Ground Ingredients Organic Oregano Leaf Powder Item#: O…
- Reason
- Potential Salmonella contamination.
- Published
- July 13, 2022
- Distribution
- U.S. distribution to the following: OR,…
FDA Recall United States Terminated Historical recordClass I
Prairie City Bakery
- Product
- Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey…
- Reason
- Salmonella. Product contains recalled Jif peanut butter as ingredient.
- Published
- July 13, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Bix Produce Company LLC
- Product
- Bix Produce Diced Spinach, Item # 15939. packaged in 2lb ba…
- Reason
- Foreign object - plastic
- Published
- July 13, 2022
- Distribution
- WI
FDA Recall United States Terminated Historical recordClass II
DANONE US LLC
- Product
- SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert S…
- Reason
- A small number of individual cones with peanut pieces were mistakenly packed into a few cartons of Salted Caramel Sundae which does not have peanuts.
- Published
- July 13, 2022
- Distribution
- AZ; CA; CO; FL; IA; KY; MA; MD; NH; NY;…
FDA Recall United States Terminated Historical recordClass I
OS Holding Inc
- Product
- Organic Oregano Ground is packed in bulk 35 lbs. cases with…
- Reason
- Ground organic oregano is recalled due to presence of Salmonella leeuwarden.
- Published
- July 13, 2022
- Distribution
- Distributed in AZ, MN, and WI.
FDA Recall Terminated Historical recordClass II
Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16
- Reason
- Defective container: defect prevents product from dispensing as intended.
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, N.Y. 11701. NDC: 50383-732-02
- Reason
- Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186 By Noven Pharmaceuticals, Inc., Miami, FL 33186. NDC 68968-5552-3
- Reason
- Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc. Camarillo, CA 93012, NDC 61152-199-99, UPC 7 69682 29101 3
- Reason
- Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC # 33342-052-44, Rx Only, MFR: Macleods Pharma USA, Inc. Plainsboro, NJ 08536
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles, Rx Only, Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-165-90 UPC 3 72789 16590 5
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets, USP 50 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-164-90 UPC 3 72789 16490 8
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets, USP 25 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-163-90 UPC 3 72789 16390 1
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Independent Beverage Company LLC
- Product
- PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWA…
- Reason
- Firm indicated that the product contains undeclared caffeine.
- Published
- July 6, 2022
- Distribution
- Product was shipped to the following sta…
FDA Recall United States Terminated Historical recordClass II
Wilton Industries Inc
- Product
- Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 71…
- Reason
- Milk contamination
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Wilton Industries Inc
- Product
- Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 71…
- Reason
- Milk contamination
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Fudgeamentals LLC
- Product
- Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)
- Reason
- made with peanut butter contaminated with Salmonella
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Fudgeamentals LLC
- Product
- 1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. 2. W…
- Reason
- made with peanut butter contaminated with Salmonella
- Published
- July 6, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Fudgeamentals LLC
- Product
- PEANUT BUTTER FUDGE BAR (24-8OZ) FUDGEAMENTALS
- Reason
- made with peanut butter contaminated with Salmonella
- Published
- July 6, 2022
- 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.
