FDA Recall United States Terminated Historical recordClass I
Houdini Inc.
- Product
- Sweets For The Season gift basket, Item No. 1081594
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,841
Class I recallsReasonable probability of serious health consequences24,366
Class II recallsTemporary or medically reversible health consequences2,892
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
2,073 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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)
- 1,714 recalls have been announced year to date.
- Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
- The highest complete period was Jun 2026 (297).
- 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 | 24,366 |
| Class I | 9,841 |
| Class III | 2,892 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,366 |
| Class I | 9,841 |
| Class III | 2,892 |
| Not Yet Classified | 2 |
FDA Recall United States Terminated Historical recordClass I
Houdini Inc.
- Product
- Tis The Season gift basket, Item No. 1084804
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Houdini Inc.
- Product
- Wooden Centerpiece gift basket, Item No. 1080571
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Houdini Inc.
- Product
- Houdini Fabric gift basket, Item No. 1072552
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Houdini Inc.
- Product
- Vintners Path Chardonnay Seasons Greetings Basket #795
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Del Dee Foods Inc.
- Product
- Hemp & Grain Co., Organic Pea Protein 80%, Net Weight 44.1 l…
- Reason
- Del Dee Foods, Inc.withdrew Lot# PP33116-0-D after receiving a report of salmonella found in two sample tests taken from product in the above lot before it reached the consumer.
- Published
- February 8, 2017
- Distribution
- US; MN, CA, NJ, WI. OUS: CANADA
FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- Caramel Apple Cake Mix (590g)
- Reason
- Possible contamination of product with Salmonella due to incorporation of powdered milk and powdered buttermilk .
- Published
- February 8, 2017
- Distribution
- MN, IN, WA, Canada
FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- 50423 Madison Hot Cocoa WIP; Production date 11/30/16
- Reason
- Possible contamination of product with Salmonella due to incorporation of powdered milk and powdered buttermilk .
- Published
- February 8, 2017
- Distribution
- MN, IN, WA, Canada
FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- Hot Cocoa, NOT FOR RETAIL SALE, Prod: 28OCT2016, BB: 28JUN20…
- Reason
- Possible contamination of product with Salmonella due to incorporation of powdered milk and powdered buttermilk .
- Published
- February 8, 2017
- Distribution
- MN, IN, WA, Canada
FDA Recall United States Terminated Historical recordClass II
Rich Products Corp
- Product
- RICH'S 1/4 Sheet White Cake with Vanilla Ice Cream Cake, KEE…
- Reason
- The product may contain undeclared walnuts from intermediate layer cake supplier.
- Published
- February 8, 2017
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Rich Products Corp
- Product
- Signature SELECT Vanilla Ice Cream & White Cake ICE CREAM CA…
- Reason
- The product may contain undeclared walnuts from intermediate layer cake supplier.
- Published
- February 8, 2017
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Rich Products Corp
- Product
- Jon Donaire Ice Cream Layer Cake, Deliciously moist white ca…
- Reason
- The product may contain undeclared walnuts from intermediate layer cake supplier.
- Published
- February 8, 2017
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Rich Products Corp
- Product
- Jon Donaire Ice Cream Layer Cake, Deliciously moist white ca…
- Reason
- The product may contain undeclared walnuts from intermediate layer cake supplier.
- Published
- February 8, 2017
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass III
Azelastine Hydrochloride Nasal Solution (Nasal Spray), 0.1% (137 mcg per spray), packaged in 30 mL bottles, Rx only, Distributed by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-0293-99
- Reason
- Defective Delivery System: out of specification result for droplet size distribution at the d90 measurement testing during the 6 month time point..
- Published
- February 1, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Mesalamine, U.S.P. [CAS 89-57-6] Cambrex Charles City, Inc. Charles City, IA packaged in double lined PE liners inside Poly-lined cardboard drums. Net weight 40 kg
- Reason
- Presence of Particulate Matter: Stainless steel in a chemical reactor dissolved into the API solution and was detected in the finished product.
- Published
- February 1, 2017
- Distribution
- Product distributed solely to the state…
FDA Recall Terminated Historical recordClass III
buPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, 60 count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India NDC 47335-0738-86
- Reason
- Failed Dissolution Specifications; 18 month stability time point
- Published
- February 1, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
buPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, a) 60 (NDC 47335-737-86), b) 100 (NDC 47335-737-88) and c) 500 (NDC 47335-737-13) count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India
- Reason
- Failed Dissolution Specifications; 18 month stability time point
- Published
- February 1, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Temozolomide Capsules, 250 mg, 5-count bottles, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA, NDC 0378-5265-98.
- Reason
- Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
- Published
- February 1, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Temozolomide Capsules, 180 mg, packaged in a) 5-count bottles (NDC 0378-5264-98), b) 14-count bottles (NDC 0378-5264-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
- Reason
- Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
- Published
- February 1, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Temozolomide Capsules, 140 mg, packaged in a) 5-count bottles (NDC 0378-5263-98), b) 14-count bottles (NDC 0378-5263-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
- Reason
- Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
- Published
- February 1, 2017
- 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.
