FDA Recall United States TerminatedTerminated: September 17, 20262026 recordClass II
JFE FRANCHISING INC
- Product
- " Dumpling Vegetable 4.5 oz…
- Reason
- Foreign Object (Glass)
- Published
- April 8, 2026
- 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 October 2026.
37,268
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,852
Class I recallsReasonable probability of serious health consequences24,397
Class II recallsTemporary or medically reversible health consequences2,897
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
2,085 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.
Filters
Metric
View
A chart of recalls grouped by month.
Download CSVSummary (Year to date)
- 1,739 recalls have been announced year to date.
- Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
- The highest complete period was Jun 2026 (300).
- Oct 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 | 24,397 |
| Class I | 9,852 |
| Class III | 2,897 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,397 |
| Class I | 9,852 |
| Class III | 2,897 |
| Not Yet Classified | 2 |
FDA Recall Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 TerminatedTerminated: April 28, 20262026 recordClass II
Albertsons Companies LLC
- Product
- Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Ad…
- Reason
- Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in coil width. Spring ends are not sharp but may be sharp if broken/ cut.
- Published
- April 1, 2026
- Distribution
- Distributed in AK, ID, CA, OR, and WA.
FDA Recall United States Ongoing2026 recordClass II
Mangalm LLC
- Product
- Tops GOLD Green Chilli Pickle NET QTY.: 31.74oz PRODUCT OF I…
- Reason
- Potential adulteration with erucic acid from mustard oil ingredient.
- Published
- April 1, 2026
- Distribution
- U.S. Distribution: CA, NV, OR, UT, WA. F…
FDA Recall United States Ongoing2026 recordClass II
Mangalm LLC
- Product
- Tops GOLD Stuffed Red Chilli Pickle NET QTY.: 31.74oz PRODUC…
- Reason
- Potential adulteration with erucic acid from mustard oil ingredient.
- Published
- April 1, 2026
- Distribution
- U.S. Distribution: CA, NV, OR, UT, WA. F…
FDA Recall United States Ongoing2026 recordClass II
Mangalm LLC
- Product
- Tops GOLD Khatta Meetha Pickle NET QTY.: 33.51oz PRODUCT OF…
- Reason
- Potential adulteration with erucic acid from mustard oil ingredient.
- Published
- April 1, 2026
- Distribution
- U.S. Distribution: CA, NV, OR, UT, WA. F…
FDA Recall United States Ongoing2026 recordClass II
Mangalm LLC
- Product
- Tops GOLD Lime Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC…
- Reason
- Potential adulteration with erucic acid from mustard oil ingredient.
- Published
- April 1, 2026
- Distribution
- U.S. Distribution: CA, NV, OR, UT, WA. F…
FDA Recall United States Ongoing2026 recordClass II
Mangalm LLC
- Product
- Tops GOLD Mango Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UP…
- Reason
- Potential adulteration with erucic acid from mustard oil ingredient.
- Published
- April 1, 2026
- Distribution
- U.S. Distribution: CA, NV, OR, UT, WA. F…
FDA Recall United States Ongoing2026 recordClass II
Mangalm LLC
- Product
- Tops GOLD Mixed Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UP…
- Reason
- Potential adulteration with erucic acid from mustard oil ingredient.
- Published
- April 1, 2026
- Distribution
- U.S. Distribution: CA, NV, OR, UT, WA. F…
FDA Recall United States TerminatedTerminated: May 11, 20262026 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…
FDA Recall United States TerminatedTerminated: June 5, 20262026 recordClass II
Pacific Coast Fresh CO
- Product
- King Harvest brand Spinach Hummus. Product is packed in 10oz…
- Reason
- Foreign material (aluminum pieces).
- Published
- April 1, 2026
- Distribution
- Distributed in OR and WA.
FDA Recall United States TerminatedTerminated: June 5, 20262026 recordClass II
Pacific Coast Fresh CO
- Product
- King Harvest brand Black Olive Hummus. Product is packed in…
- Reason
- Foreign material (aluminum pieces).
- Published
- April 1, 2026
- Distribution
- Distributed in OR and WA.
FDA Recall United States TerminatedTerminated: June 5, 20262026 recordClass II
Pacific Coast Fresh CO
- Product
- King Harvest brand Balsamic Hummus. Product is packed in 10o…
- Reason
- Foreign material (aluminum pieces).
- Published
- April 1, 2026
- Distribution
- Distributed in OR and WA.
FDA Recall United States TerminatedTerminated: June 5, 20262026 recordClass II
Pacific Coast Fresh CO
- Product
- King Harvest brand Sundried Tomato Hummus. Product is packed…
- Reason
- Foreign material (aluminum pieces).
- Published
- April 1, 2026
- Distribution
- Distributed in OR and WA.
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.
