FDA Recall United States Terminated Historical recordClass II
Newly Weds Foods Inc
- Product
- B10209 Cracker Meal X1, NET WT 50 LBS, Manufactured By: New…
- Reason
- Product may contain undeclared milk.
- Published
- July 26, 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.
37,136
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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/berlin-seeds-recalls-alfalfa-sprouting-seed-because-possible-health-riskPublished September 23, 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 United States Terminated Historical recordClass II
Newly Weds Foods Inc
- Product
- A59036 Breader X2, NET WT 50 LBS, Manufactured By: Newly We…
- Reason
- Product may contain undeclared milk.
- Published
- July 26, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Newly Weds Foods Inc
- Product
- A55046 Breader X1, NET WT 25 LBS, Manufactured By: Newly We…
- Reason
- Product may contain undeclared milk.
- Published
- July 26, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Newly Weds Foods Inc
- Product
- B30434, BREADER, NET WT 50 LBS, Manufactured By: Newly Wed…
- Reason
- Product may contain undeclared milk.
- Published
- July 26, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
New England Natural Bakers, Inc.
- Product
- Millville Fruit & Nut Whole Grain Granola - 16 oz .carton D…
- Reason
- Product may be contaminated with Listeria monocytogenes
- Published
- July 26, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
New England Natural Bakers, Inc.
- Product
- Evoke Organic Muesli Classic Swiss 12 oz. pouch UPC: 85330…
- Reason
- Product may be contaminated with Listeria monocytogenes
- Published
- July 26, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India, NDC: 68180-647-06
- Reason
- Failed Dissolution Specifications: out of specification observed in dissolution testing at 3 month long term stability study.
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
0.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B1309, NDC: 0338-0049-38
- Reason
- Lack of Assurance of Sterility: Bags have the potential to leak.
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B0089, NDC: 0338-0017-38
- Reason
- Lack of Assurance of Sterility: Bags have the potential to leak.
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
LabidaMAX Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY --- UPC Code 680474228904
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
ZRECT for Women Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229055
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
ENHANCEROL Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
BIGnHARD Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229062
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
TORNADO Male Enhancement Herbal Dietary Supplement Capsules, Over 4000 mg value, supplied in 2, 4 and 10 count packages, Made in USA Distributed by American Health Supplements, Chicago, Illinois --- UPC Code 680474228959
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
RECTALIS Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY --- UPC Code 680474228782
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Xrect Male Enhancement Herbal Dietary Supplement Capsules, 500 mg supplied in 2, 4 and 10 count packages, Distributed by Organic Herbal Supply, Roseville, CA ---- UPC Code 680474015795
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
ZRECT Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 852675999451
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Cummor Natural Male Enhancement, Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Naturally Hard Supplements, Reno, NV --- UPC code #680474229116
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules, supplied in 2, 4 and 10 count packages, Distributed by AH Distribution, DelRay, Beach, FL ---- UPC Code 680474229260
- Reason
- Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
- Published
- July 19, 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.
