FDA Recall United States Terminated Historical recordClass II
FRUSELVA USA
- Product
- Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Pur…
- Reason
- elevated level of lead
- Published
- April 9, 2025
- Distribution
- Nationwide
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.
37,061
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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 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.
Filters
Metric
View
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 II
Seattle Homemade Thai LLC
- Product
- Panang Curry Tofu Vegan GF is a refrigerated and ready to ea…
- Reason
- Label declares tofu but it does not declare soy.
- Published
- April 9, 2025
- Distribution
- Distributed in WA.
FDA Recall United States Terminated Historical recordClass II
Seabear Company
- Product
- SeaBear Smokedhouse Alehouse Clam Chowder is packaged in ret…
- Reason
- Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
- Published
- April 9, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Seabear Company
- Product
- SeaBear Smokedhouse Salmon Chowder is packaged in flexible r…
- Reason
- Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
- Published
- April 9, 2025
- Distribution
- Nationwide
FDA Recall United States Completed Historical recordClass II
Nestle-USA, Inc. (Corporate Office)
- Product
- Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g),…
- Reason
- Potential foreign material (wood-like material)
- Published
- April 9, 2025
- Distribution
- Distributors and retailers in the follow…
FDA Recall United States Completed Historical recordClass II
Nestle-USA, Inc. (Corporate Office)
- Product
- Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g…
- Reason
- Potential foreign material (wood-like material)
- Published
- April 9, 2025
- Distribution
- Distributors and retailers in the follow…
FDA Recall United States Completed Historical recordClass II
Nestle-USA, Inc. (Corporate Office)
- Product
- Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283…
- Reason
- Potential foreign material (wood-like material)
- Published
- April 9, 2025
- Distribution
- Distributors and retailers in the follow…
FDA Recall Ongoing Historical recordClass II
8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL (1 mEq/mL), 25 x 50 mL Single Dose Vials per carton, For Intravenous Use Only, Rx Only, Manufactured by: Exela Pharma Sciences, LLC, Lenoir, NC 28645. NDC Inner Vial: 51754-5001-1; NDC Carton: 51754-5001-4
- Reason
- Lack of Assurance of Sterility
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 kettle style Neti Pot, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00102 7
- Reason
- Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg) for Nasal Wash System, 60-count All Natural USP Grade Saline Packets, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00103 4
- Reason
- Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 Soft tip Squeeze Bottle, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00104 1
- Reason
- Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
babyganics, Sheer Blend, SPF 50 Mineral Sunscreen Fragrance Free (zinc oxide 20%), a) 1.7 FL OZ (50 mL) bottle, UPC 810035921658, b) 8 FL OZ (236 mL) bottle, UPC 810035921382, Dist. by KAS Direct, LLC, 1525 Howe St., Racine, WI 53403, Made in Canada.
- Reason
- Failed stability specifications: during routine stability monitoring quality concerns were identified. Physical separation for ingredients was observed.
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine HCl 200 mg/100 mL (2 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, Tx 77478. NDC: 70092-1259-75
- Reason
- Lack of Assurance of Sterility
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, Tx 77478. NDC: 70092-1255-75
- Reason
- Lack of Assurance of Sterility
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine HCl 100 mg/100 mL (1 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, Tx 77478. NDC: 70092-1255-75
- Reason
- Lack of Assurance of Sterility
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Testosterone Gel 1%, 5 grams, 30 Unit-dose Packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 64380-152-02
- Reason
- Presence of foreign substance: Presence of Benzene.
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Testosterone Gel 1%, 2.5 grams, 30 Unit-dose packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 64380-151-02
- Reason
- Presence of foreign substance: Presence of Benzene.
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG, 180 TABLETS, Packaged BY: A-S Medication Solutions, Libertyville, IL 60048 NDC 50090-1494-3.
- Reason
- Presence of Foreign Tablets/Capsules.
- Published
- April 2, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass III
U.S. Tov, Inc. dba U.S. Trading Company
- Product
- DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily…
- Reason
- Undeclared sulfites
- Published
- April 2, 2025
- Distribution
- Multiple states
FDA Recall Ongoing Historical recordClass II
Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-443-20.
- Reason
- Super-Potent Drug: Out of specification potency results were obtained.
- Published
- March 26, 2025
- 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.
