FDA Recall Terminated Historical recordClass II
Altera Handset NDC 83490-0678-05 56 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
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.
37,142
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
Cosentyx 150 mg/mL PFS 300 mg Dose NDC 00078-0639-98, 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Taltz 80 mg/mL Pen 1-pk NDC 00002-1445-11 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Otezla 30 mg tablet NDC 59572-0631-06 30 days supply;
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Pulmicort Respules 0.5 mg/2mL s, 30 days supply, NDC 00186-1989-04
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Polyethylene Glycol 3350, powder, for solution 527g BRE, Rx Only, 28 days supply, NDC 51991-0457-57
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Pediasure Liq. Vanilla G+G (CAN) #24 24 days supply, NDC 70074-0558-98
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Kalydeco 150 mg tablet blister, 28 days supply, Rx Only, 39183, NDC 51167-0200-01
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Humira Pen Sub-q Kit a.) 40 mg/0.8 mL (NDC 00074-4339-02); Humira Pen Psor Kit b.) 40 mg/0.8 mL (NDC 00074-4339-07) 28 day supply, Rx Only,
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited Bachupally-500 090 India\ NDC 55111-468-01
- Reason
- Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.
- Published
- May 16, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Badger Botanicals LLC
- Product
- Acadica Kratom: Green Hulu 2 Kratom, 250g bags
- Reason
- Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
- Published
- May 16, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Badger Botanicals LLC
- Product
- Acadica Kratom: Red Hulu 2, 250g bags
- Reason
- Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
- Published
- May 16, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Badger Botanicals LLC
- Product
- Acadica Kratom: Green Suma, 250g bags
- Reason
- Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
- Published
- May 16, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Badger Botanicals LLC
- Product
- Acadica Kratom: Red Suma 250g bags
- Reason
- Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
- Published
- May 16, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Maya Distribution, LLC
- Product
- Dragon Bali Kratom Powder: 60g Bottle. Dragon Bali Kratom Ca…
- Reason
- Samples collected by public health officials found the presence of Salmonella.
- Published
- May 16, 2018
- Distribution
- Recalled product was distributed to reta…
FDA Recall United States Terminated Historical recordClass I
Maya Distribution, LLC
- Product
- Dragon Maeng Da Kratom Powder: 60 g and 150 g bottle. Dragon…
- Reason
- Samples collected by public health officials found the presence of Salmonella.
- Published
- May 16, 2018
- Distribution
- Recalled product was distributed to reta…
FDA Recall United States Terminated Historical recordClass I
Maya Distribution, LLC
- Product
- Dragon Malaysian Kratom Powder: 150 g bottle. Dragon Malaysi…
- Reason
- Samples collected by public health officials found the presence of Salmonella.
- Published
- May 16, 2018
- Distribution
- Recalled product was distributed to reta…
FDA Recall United States Terminated Historical recordClass I
Maya Distribution, LLC
- Product
- Dragon Ultra Ehanced Indo Extract 4-ct x 500 mg capsules in…
- Reason
- Samples collected by public health officials found the presence of Salmonella.
- Published
- May 16, 2018
- Distribution
- Recalled product was distributed to reta…
FDA Recall United States Terminated Historical recordClass I
Stonewall Kitchen, LLC
- Product
- STONEWALL KITCHEN Basil Pesto Aioli Net Weight Net 10.25 oz.…
- Reason
- Product may contain undeclared eggs.
- Published
- May 16, 2018
- Distribution
- Multiple states
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.
