FDA Recall Terminated Historical recordClass II
Dexamethasone Sodium Phosphate in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- 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
Adenosine Injection in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Succinylcholine Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ketamine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Potassium Chloride in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Fentanyl Citrate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Lidocaine HCl in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Morphine Sulfate in 5% Dextrose in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Morphine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Midazolam HCl in 5% Dextrose in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Midazolam HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
HYDROmorphone HCl Injection in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ephedrine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Fentanyl Citrate and Bupivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Fentanyl Citrate and Ropivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Bupivacaine HCl in 0.9% Sodium Chloride in all doses, all strengths, and packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
HYDROmorphone HCl in Sodium Chloride 0.9% in all doses, all strengths, and all packaging.
- Reason
- Lack of sterility assurance.
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Metformin Hydrochloride Tablets, USP 1000 mg, 500-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc. 2400 Route 130 North Dayton, NJ 08810, Manufactured by: Aurobindo Pharma Limited Unit -VII (SEZ)) Mahabubnagar (Dt)_509302 India, NDC 65862-010-05.
- Reason
- Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of Metformin HCl 1000mg
- Published
- February 28, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
National Frozen Foods Corporation--Seattle
- Product
- IQF blend product sold as Not Ready To Eat (NRTE) product fo…
- Reason
- Frozen blend vegetable product containing green beans are recalled due to a potential contamination with Listeria monocytogenes.
- Published
- February 28, 2018
- Distribution
- distributed in AK, AR, AZ, CA, CO, FL, I…
FDA Recall United States Terminated Historical recordClass II
National Frozen Foods Corporation--Seattle
- Product
- IQF Green beans, sold as Not Ready To Eat (NRTE) product for…
- Reason
- Frozen green beans are recalled due to a potential contamination with Listeria monocytogenes.
- Published
- February 28, 2018
- Distribution
- distributed in AK, AR, AZ, CA, CO, FL, I…
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.
