FDA Recall United States Terminated Historical recordClass II
Dean Foods, Inc.
- Product
- Baskin Robbins Mint Chocolate Chip
- Reason
- Product may contain unlabeled coconut.
- Published
- June 13, 2018
- Distribution
- Nationwide
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,799
Class I recallsReasonable probability of serious health consequences24,349
Class II recallsTemporary or medically reversible health consequences2,891
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/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026
Download matching recalls as CSV
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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 | 24,349 |
| Class I | 9,799 |
| Class III | 2,891 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,349 |
| Class I | 9,799 |
| Class III | 2,891 |
| Not Yet Classified | 1 |
FDA Recall United States Terminated Historical recordClass I
Lake Michigan Distilling Co LLC
- Product
- Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, M…
- Reason
- Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a voluntary recall of Ethanol Extraction s 190 Proof Non-Denatured Grain Alcohol due to contamination with methanol which could cause serious injury or death if consumed.
- Published
- June 13, 2018
- Distribution
- Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…
FDA Recall United States Terminated Historical recordClass II
The C.F. Sauer Company
- Product
- Code - Red Pepper Seasoning (21 oz.) Net Weight: 21 oz., N…
- Reason
- The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.
- Published
- June 13, 2018
- Distribution
- Product has been distributed to: Georgia…
FDA Recall United States Terminated Historical recordClass II
The C.F. Sauer Company
- Product
- Premium - Recipe Red Pepper Seasoning (21 oz.) Net Weight:…
- Reason
- The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.
- Published
- June 13, 2018
- Distribution
- Product has been distributed to: Georgia…
FDA Recall United States Terminated Historical recordClass II
The C.F. Sauer Company
- Product
- Pocahontas - Red Pepper Seasoning (21 oz.) Net Weight: 21 o…
- Reason
- The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.
- Published
- June 13, 2018
- Distribution
- Product has been distributed to: Georgia…
FDA Recall United States Terminated Historical recordClass II
The C.F. Sauer Company
- Product
- Blue Mountain Valley - Red Pepper Seasoning (21 oz.) Net We…
- Reason
- The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.
- Published
- June 13, 2018
- Distribution
- Product has been distributed to: Georgia…
FDA Recall United States Terminated Historical recordClass II
The C.F. Sauer Company
- Product
- Sauer - Red Pepper Seasoning (21 oz.) Net Weight: 21 oz.,…
- Reason
- The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.
- Published
- June 13, 2018
- Distribution
- Product has been distributed to: Georgia…
FDA Recall Terminated Historical recordClass I
7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC 601577513148
- Reason
- Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
- Published
- June 6, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857
- Reason
- Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
- Published
- June 6, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Morski Brands Inc. dba Dawn's Fresh Foods
- Product
- Sully's Potato Salad, Mfg. No. 10125, Net Wt. 10 lbs. (4.54k…
- Reason
- Product has the potential to be contaminated with Listeria monocytogenes.
- Published
- June 6, 2018
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Morski Brands Inc. dba Dawn's Fresh Foods
- Product
- Finest Traditions Deluxe Potato Salad, Packaged into the fol…
- Reason
- Product has the potential to be contaminated with Listeria monocytogenes.
- Published
- June 6, 2018
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Morski Brands Inc. dba Dawn's Fresh Foods
- Product
- Dawn's Foods Deluxe Potato Salad Mfg. No. 20114, Net Wt. 30…
- Reason
- Product has the potential to be contaminated with Listeria monocytogenes.
- Published
- June 6, 2018
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Morski Brands Inc. dba Dawn's Fresh Foods
- Product
- Terry's Potato Salad, Packaged into the following sized cont…
- Reason
- Product has the potential to be contaminated with Listeria monocytogenes.
- Published
- June 6, 2018
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Ziyad Brothers Importing, Inc.
- Product
- Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glas…
- Reason
- Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8 oz. 16 oz., 1/2 gallon and 32 oz. sizes due to potential contamination with Salmonella.
- Published
- June 6, 2018
- Distribution
- Domestic: AL, AR, AZ, CA, CT, DE, FL, GA…
FDA Recall Terminated Historical recordClass II
My Way (levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202; Manufactured by: Lupin Limited, Pithampur (M.P.) - 454 775, INDIA, UPC 3 68180 85212 4.
- Reason
- Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive appropriate regulatory approval prior to release.
- Published
- May 30, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
My Way (Levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, GAVIS Pharmaceuticals, A Lupin Group Company; Mfg. for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, UPC 3 43386-622-31 3.
- Reason
- Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive appropriate regulatory approval prior to release.
- Published
- May 30, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
screamin' menthol (menthol) Pain Relieving Gel, 4%, packaged in a) 2 OZ (57g) tubes, UPC 7 50263 80062 5; b) 5 oz. (141g) tubes, UPC 7 50263 80006 9; and c) 16 oz. (454g) bottles, UPC 7 50263 80066 3; MFD FOR: Toast Products, 400 Sproul Street, Pittsburgh, PA 15136; NDC 52099-8010.
- Reason
- CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.
- Published
- May 30, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg, 60-count bottle, Rx Only, Manufactured by: Cipla Ltd., India; For: EAGLE PHARMACEUTICALS, INC., Woodcliff Lake, NJ 07677 USA, NDC 42367-111-06.
- Reason
- Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol 75 mg/0.2 mg contained Diclofenac Sodium and Misoprostol 50 mg/0.2 mg tablets.
- Published
- May 30, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Loxapine Capsules, USP 50 mg, packaged in 100 Unit Dose capsules, Rx only, Manufactured by Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. NDC 51079-903-20.
- Reason
- GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination
- Published
- May 30, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Loxapine Capsules, USP 25 mg, packaged in 100 Unit Dose Capsules, Rx only, Manufactured by Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. NDC 51079-902-20
- Reason
- GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination
- Published
- May 30, 2018
- 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.
