FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- Fruit Fresh Up Raspberry Dip (7oz)
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- 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.
37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,793
Class I recallsReasonable probability of serious health consequences24,343
Class II recallsTemporary or medically reversible health consequences2,887
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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- 1. Lexington Co-op 10oz Honeydew Chunk (2/cs) 2. EDU Kids…
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- Fresh Harvest Small veggie platter w/ranch 64779300337
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- 1. Fresh Harvest Small fruit platter w/raspberry dip
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- All BBD 03/05/22 through 03/23/2022 1. Wegmans 32oz Cantal…
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- 1. Wegmans 32oz Melon Trio 2.Fresh Harvest 18oz Melon Trio…
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- 1. Wegmans 32oz Pineapple Spears 2. Fresh Harvest 18oz Pine…
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Fruit Fresh Up, Inc.
- Product
- 1. Wegmans 10oz Watermelon Chunks 2. Wegmans 32oz Watermel…
- Reason
- may be contaminated with Listeria monocytogenes
- Published
- April 13, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass III
Sauer Brands Inc - New Century
- Product
- Caesar dressing in a 1.5 oz pouch
- Reason
- Undeclared Allergen - Soy
- Published
- April 13, 2022
- Distribution
- Institutional/Foodservice accounts in mu…
FDA Recall Terminated Historical recordClass II
Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090, India, NDC 55111-399-90.
- Reason
- Failed Dissolution Specifications; during long term stability testing.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Lansoprazole Delayed-Release Capsules, USP, 15 mg, a) 30-count bottle, (NDC 55111-398-30), b) 90-count bottle, (55111-398-90), Rx Only, Manufactured. By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090, India
- Reason
- Failed Dissolution Specifications; during long term stability testing.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Glycopyrrolate Tablets, USP, 1 mg, 100-count bottle, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, NDC 13107-014-01.
- Reason
- Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable, Packaged in a multi dose 10ML vial, Formula ID 127492, APS Pharmacy
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable, Packaged in a multi dose 10ML vial, Formula ID 76681, APS Pharmacy
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable, Packaged in a multi dose 10ml vial, Formula ID 115498, APS Pharmacy
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable, Packaged in a multi dose 10ML vial, as a) 5 ML Formula ID 115678; b) 10 ML Formula ID 115498, APS Pharmacy
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML; Packaged in a multi dose 10ML vial, as a) (CA) 4 ML Formula ID 136164; b) (RM) 10 ML Formula ID 115962; APS Phar
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
TESTOSTERONE CYPIONATE/ANASTROZOLE *GS* OIL 200MG/1MG/ML Injectable, Packaged in a multi dose 10ML vial, as a) 4 ML Formula ID 115387; b) (RM) 10 ML Formula ID 115125; APS Pharmacy
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
GONADORELIN (5ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID132227, APS Pharmacy
- Reason
- Lack of sterility assurance.
- Published
- April 6, 2022
- 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.
