FDA Recall United States Ongoing 2026 recordClass II
AZ Gems, Inc.
- Product
- Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial…
- Reason
- elevated levels of chloramphenicol in frozen shrimp
- Published
- January 21, 2026
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,060
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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 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 | 24,313 |
| 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 2026 recordClass II
WhiteWave - Louisville Pilot Plant
- Product
- So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, N…
- Reason
- Foreign material
- Published
- January 21, 2026
- Distribution
- Nationwide
FDA Recall United States Completed 2026 recordClass II
House Of Flavors, Inc.
- Product
- 1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6
- Reason
- Undeclared soy lecithin
- Published
- January 21, 2026
- Distribution
- AL AZ CT GA IA IL IN KY MI MN MO NC NJ N…
FDA Recall United States Completed 2026 recordClass II
House Of Flavors, Inc.
- Product
- 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8
- Reason
- Undeclared soy lecithin
- Published
- January 21, 2026
- Distribution
- AL AZ CT GA IA IL IN KY MI MN MO NC NJ N…
FDA Recall Ongoing 2026 recordClass II
Rosuvastatin Tablets, USP, 10 mg, Rx Only, 50 Tablets (5 x 10) Unit Dose per carton, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 50268-709-15
- Reason
- Out of specification for dissolution.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass I
ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887
- Reason
- Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass I
ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863
- Reason
- Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0522-01. Case label: SpecGx LLC, NDC 0406052201, Exp. 2027/03, Lot: 0522J23493
- Reason
- Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01.
- Reason
- Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
ORL Kids Natural Toothpaste, Bubblegum Flavor, 4 oz (120ml), ORL Labs, LLC, Scottsdale, Arizona USA
- Reason
- cGMP Deviations
- Published
- January 14, 2026
- Distribution
- AZ only
FDA Recall Ongoing 2026 recordClass II
ORL Kids Mouthwash, Bubblegum Flavor, 16.9 oz. (500ml) per bottle, ORL Labs, LLC, Scottsdale, Arizona USA
- Reason
- cGMP Deviations
- Published
- January 14, 2026
- Distribution
- AZ only
FDA Recall Ongoing 2026 recordClass II
Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852. NDC 71384-746-06.
- Reason
- Presence of particulate matter - Glass like particles.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, 0.4 mg/mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-513-01.
- Reason
- Presence of particulate matter - Glass like particles.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-512-0.1
- Reason
- Presence of particulate matter - Glass like particles.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass III
Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-176-30
- Reason
- Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall United States Ongoing 2026 recordClass II
MAYEJ COMERCIALIZADORA S. de R.L. de C.V.
- Product
- Italian Parsley packaged in 24lb boxes, 40 bunches per box i…
- Reason
- pathogen Cyclospora cayetanensis
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall United States Terminated 2026 recordClass II
ZIYAD BROTHERS IMPORTING
- Product
- Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 re…
- Reason
- May contain partially hydrogenated oils
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall United States Terminated 2026 recordClass II
ZIYAD BROTHERS IMPORTING
- Product
- Baraka French Style Puff Pastry 1lb and 1.5lbs sizes, UPCs 8…
- Reason
- May contain partially hydrogenated oils
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall United States Terminated 2026 recordClass II
McCain Foods USA Inc
- Product
- Sysco Imperial Potato Tater Barrel, item number 1000006067.…
- Reason
- Clear hard plastic fragments.
- Published
- January 14, 2026
- Distribution
- Distributed in AK, AZ, CA, CO, FL, HI, I…
FDA Recall United States Terminated 2026 recordClass II
McCain Foods USA Inc
- Product
- Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. F…
- Reason
- Clear hard plastic fragments.
- Published
- January 14, 2026
- Distribution
- Distributed in AK, AZ, CA, CO, FL, HI, 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.
