FDA Recall United States Ongoing 2026 recordClass II
JFE FRANCHISING INC
- Product
- " Dumpling Vegetable 4.5 oz…
- Reason
- Foreign Object (Glass)
- Published
- April 8, 2026
- Distribution
- Multiple states
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,059
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
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
TG FOODS INC
- Product
- Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Po…
- Reason
- The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.
- Published
- April 8, 2026
- Distribution
- Multiple states
FDA Recall United States Terminated 2026 recordClass III
Pocas International Corp.
- Product
- POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA 12 X 13.8OZ
- Reason
- Packaging integrity issue that may compromise product quality .
- Published
- April 8, 2026
- Distribution
- The product was distributed to the follo…
FDA Recall United States Terminated 2026 recordClass III
Pocas International Corp.
- Product
- POPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA 12 X 13.8OZ
- Reason
- Packaging integrity issue that may compromise product quality .
- Published
- April 8, 2026
- Distribution
- The product was distributed to the follo…
FDA Recall United States Terminated 2026 recordClass III
Pocas International Corp.
- Product
- POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ
- Reason
- Packaging integrity issue that may compromise product quality .
- Published
- April 8, 2026
- Distribution
- The product was distributed to the follo…
FDA Recall United States Terminated 2026 recordClass III
Pocas International Corp.
- Product
- POPPING BOBA RTD PEACH OOLONG TEA 12 X 13.8OZ
- Reason
- Packaging integrity issue that may compromise product quality .
- Published
- April 8, 2026
- Distribution
- The product was distributed to the follo…
FDA Recall Ongoing 2026 recordClass II
Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217.
- Reason
- Failed tablet specifications.
- Published
- April 1, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9262-08.
- Reason
- Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
- Published
- April 1, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 20 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9259-08.
- Reason
- Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
- Published
- April 1, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 10 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9257-08.
- Reason
- Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
- Published
- April 1, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44
- Reason
- Subpotent Drug
- Published
- April 1, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03.
- Reason
- Lack of Assurance of Sterility
- Published
- April 1, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass III
Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35
- Reason
- Failed Tablet/Capsule Specifications
- Published
- April 1, 2026
- Distribution
- Nationwide
FDA Recall United States Completed 2026 recordClass I
Distribuidora de Alimentos Sendero LLC
- Product
- Doraditas de Azucar UPC 5901234123457
- Reason
- Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
- Published
- April 1, 2026
- Distribution
- Texas
FDA Recall United States Completed 2026 recordClass I
Distribuidora de Alimentos Sendero LLC
- Product
- Gorditas de Azucar UPC 860010238134
- Reason
- Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
- Published
- April 1, 2026
- Distribution
- Texas
FDA Recall United States Ongoing 2026 recordClass I
Siluetaya, LLC
- Product
- SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottl…
- Reason
- Product contains yellow oleander
- Published
- April 1, 2026
- Distribution
- Product was distributed directly to cons…
FDA Recall United States Ongoing 2026 recordClass II
Rose and Shore, Inc.
- Product
- 14" Margarita Thin Crust Pizza; 8 units per case. Keep Froze…
- Reason
- potential foreign object (metal pieces) in ingredient (Tomatoes)
- Published
- April 1, 2026
- Distribution
- Product was distributed to a single reta…
FDA Recall United States Ongoing 2026 recordClass II
Bakkavor
- Product
- Roasted Tomato Parmesan Focaccia Bread sold under the brand…
- Reason
- Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
- Published
- April 1, 2026
- Distribution
- Product was shipped to the following sta…
FDA Recall United States Ongoing 2026 recordClass II
Bakkavor
- Product
- Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8…
- Reason
- Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
- Published
- April 1, 2026
- Distribution
- Product was shipped to the following sta…
FDA Recall United States Terminated 2026 recordClass II
Savannah Bee Company Inc.
- Product
- SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (4…
- Reason
- Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the product inside the bottle is a different flavor of BBQ sauce. After investigation, the firm determined that the product in the bottle is their Honey BBQ Sauce "Sweet". The BBQ sauce "Sweet" contains wheat and soy which is not listed on the BBQ Sauce "Mustard" label.
- Published
- April 1, 2026
- Distribution
- Product was shipped to the following sta…
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.
