FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- Vegetarian Pia Cake Pandan Durian, 14oz (400g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
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.
37,066
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 Historical recordClass I
LQNN Inc.
- Product
- Vegetarian Pia Cake Mung Bean Pineapple, 14oz (400g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- Vegetarian Pia Cake Mungbean Durian, 14oz (400g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- BANH PIA Hopia Cake Mungbean Durian, 9.7oz (275g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- Vegetarian Pia Cake Black Sesame Durian, 14oz (400g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- BANH Ba Xa Lady Cake, 260g
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- Vegetarian Pia Cake Taro Durian, 14 oz (400g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- Vegetarian Pia Cake Mung Bean Pumpkin, 14 oz (400g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
LQNN Inc.
- Product
- BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g)
- Reason
- Undeclared allergen; egg
- Published
- March 13, 2024
- Distribution
- U.S. distribution to customers in: Alaba…
FDA Recall United States Terminated Historical recordClass I
Woolery Enterprises, Inc. dba Will's Fresh Foods
- Product
- Will's Fresh Foods Street Corn Salad
- Reason
- L. mono contamination
- Published
- March 13, 2024
- Distribution
- U.S. distribution to the following: CA…
FDA Recall Ongoing Historical recordClass II
Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42
- Reason
- Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Moxifloxacin 5mg/ml, 1 ml in a Single- Dose Vial, Rx Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-097-42
- Reason
- Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42
- Reason
- Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
7 Eleven FOR GAS ISLAND USE ONLY, Hand Sanitizer, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 330 Gal. cases, Distributed by: Magnus, 16005 Gateway Drive, Suite 300, Frisco, TX 75033
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G cases, mountain spring scent, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471.
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
FDA Recall Completed Historical recordClass II
Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1,680mg, This packet contains 40mg of omeprazole and 1,680mg of sodium bicarbonate, Directions for Use: Empty packet contents into a small cup containing 1 to 2 tablespoons of WATER. DO NOT USE OTHER LIQUIDS OR FOODS. Stir well and drink immediately. Rx Only, Distributed by: Oceanside Pharmaceuticals, a division of Bausch Health US, LLC, Bridgewater, NJ 08807, NDC 68682-991-30.
- Reason
- Subpotent Drug: Out of specification for assay
- Published
- March 6, 2024
- Distribution
- Nationwide
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.
