FDA Recall United States Terminated Historical recordClass I
Willamette Hazelnut, Inc.
- Product
- SW Texas Nut Blend, Item #5180819, Packed in cardboard box w…
- Reason
- Undeclared Almonds and Cashews
- Published
- May 24, 2023
- Distribution
- Distributed in OR
Data Explorer
Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.
Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,786
Class I recallsReasonable probability of serious health consequences24,313
Class II recallsTemporary or medically reversible health consequences2,876
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
CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.
Filters
Metric
View
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 | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
FDA Recall United States Terminated Historical recordClass I
Willamette Hazelnut, Inc.
- Product
- Oregon Nut Blend, Item # 5180808, Packed in cardboard box wi…
- Reason
- Undeclared Almonds and Cashews
- Published
- May 24, 2023
- Distribution
- Distributed in OR
FDA Recall United States Terminated Historical recordClass II
REAL GREEK LLC
- Product
- The Vanilla Bean Greek Yogurt 4oz cup is part of the 12-Pack…
- Reason
- Undeclared egg. Lemon Curd yogurt was mis-labeled as Vanilla Bean yogurt and egg is not declared on Vanilla Bean yogurt label.
- Published
- May 24, 2023
- Distribution
- Distributed in Alaska, Oregon, and Washi…
FDA Recall United States Terminated Historical recordClass III
Origami Catering, LLC
- Product
- Wakame Seaweed Salad, ready to eat product. Net Weight: 4.5o…
- Reason
- Soy Sauce (Soy and Wheat) are declared in the Ingredients statement of the Wakame Seaweed Salad, but the Contains statement declares Soy and Sesame (no wheat).
- Published
- May 24, 2023
- Distribution
- Distributed in Oregon and Washington.
FDA Recall United States Terminated Historical recordClass II
Big Bold Health Holdings Inc
- Product
- Microbiome Rejuvenate dietary supplement, 60 capsules per bo…
- Reason
- Glass fragments.
- Published
- May 24, 2023
- Distribution
- Nationwide
FDA Recall United States Ongoing Historical recordClass I
SUMMIT NATURALS INC
- Product
- Highkey Soft Baked MINI TREATS BIRTHDAY CAKE NET WT 2 OZ (57…
- Reason
- The firm was notified that a consumer had an allergic reaction to their product. The product did not list egg on the label.
- Published
- May 24, 2023
- Distribution
- Product was shipped to the following sta…
FDA Recall United States Ongoing Historical recordClass I
SUMMIT NATURALS INC
- Product
- Highkey soft baked MINI TREATS BANANA NUT MUFFIN NET WT 2 OZ…
- Reason
- The firm was notified that a consumer had an allergic reaction to their product. The product did not list egg on the label.
- Published
- May 24, 2023
- Distribution
- Product was shipped to the following sta…
FDA Recall Terminated Historical recordClass III
Gabapentin Tablets, USP 600 mg, packaged in Cartons of 100 tablets (10 tablets per blister pack x 10), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. East Windsor, NJ 08520 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA, NDC 0904-6823-61
- Reason
- Product mixup: one foreign tablet found in product.
- Published
- May 17, 2023
- Distribution
- Nationwide
FDA Recall Completed Historical recordClass II
Calcitonin Salmon (synthetic origin) Nasal Spray, 2200 USP Calcitonin Salmon Units/mL, 200 USP Calcitonin Salmon Units/spray, 3.7 mL bottle, Rx only, Manufactured by: Apotex Corp., Toronto, Ontario, Canada, M9L 1T9, NDC 60505-0823-6
- Reason
- Presence of Foreign Substance: Glass splinter particle entrapped inside the pump ball seat rendered the pump inoperable.
- Published
- May 17, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
Atovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India, NDC# 31722-629-21.
- Reason
- Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.
- Published
- May 17, 2023
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Euro-Pharma
- Product
- Multiple Vitamin B Capsules, 60 Capsules, Biologically Activ…
- Reason
- undeclared allergen (milk)
- Published
- May 17, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
- Reason
- Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
- Reason
- Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.
- Reason
- Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Advil Liqui-Gels Solubilized Ibuprofen Capsules, 200 mg Pain Reliever/Fever Reducer (NSAID) a) 20-count Liquid Filled Capsule bottles; b) 40-count Liquid Filled Capsule bottles.
- Reason
- CGMP deviation: product outside labeled storage temperature requirements.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Advil Dual Action with Acetaminophen Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg Tablets Pain Reliever, 36 Caplets bottles
- Reason
- CGMP deviation: product outside labeled storage temperature requirements.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets
- Reason
- CGMP deviation: product outside labeled storage temperature requirements.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets.
- Reason
- CGMP deviation: product outside labeled storage temperature requirements.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Simvastatin USP 40 mg, Rx only, Intas Pharm. Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottle (NDC 43063-0726-30) b) 90 count-bottle (NDC 43063-0726-90)
- Reason
- CGMP deviations.
- Published
- May 10, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Simvastatin USP 20 mg, Rx only, Intas Pharm. Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottles (NDC 43063-008-30), b) 90 count-bottles (NDC: 43063-0008-90)
- Reason
- CGMP deviations.
- Published
- May 10, 2023
- 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.
