FDA Recall United States OngoingHistorical recordClass I
Piggie Park Enterprises Inc
- Product
- Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bott…
- Reason
- Undeclared soy and wheat ingredients
- Published
- April 4, 2018
- Distribution
- Nationwide
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.
37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,872
Class I recallsReasonable probability of serious health consequences24,509
Class II recallsTemporary or medically reversible health consequences2,932
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
2,096 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026
Download matching recalls as CSV
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A chart of recalls grouped by month.
Download CSVSummary (Year to date)
- 1,956 recalls have been announced year to date.
- Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
- The highest complete period was Jun 2026 (300).
- Nov 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 | 24,509 |
| Class I | 9,872 |
| Class III | 2,932 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,509 |
| Class I | 9,872 |
| Class III | 2,932 |
| Not Yet Classified | 2 |
FDA Recall United States TerminatedTerminated: March 27, 2018Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Wegmans Assorted Gyoza (Dumplings), Family Pack, 17 oz. UP…
- Reason
- The product is labeled as Thai Chili Sauce. The product actually contains Spicy Sauce which contains undeclared egg.
- Published
- April 4, 2018
- Distribution
- Wegmans Stores in NY, NJ, PA, VA, MD and…
FDA Recall United States TerminatedTerminated: March 27, 2018Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Wegmans Avocado Summer Roll, 2 Pack, 5 oz. UPC: 2-48762-0000…
- Reason
- The product is labeled as Thai Chili Sauce. The product actually contains Spicy Sauce which contains undeclared egg.
- Published
- April 4, 2018
- Distribution
- Wegmans Stores in NY, NJ, PA, VA, MD and…
FDA Recall United States TerminatedTerminated: March 27, 2018Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. (UPC 7-66630-9802…
- Reason
- The product is labeled as Thai Chili Sauce. The product actually contains Spicy Sauce which contains undeclared egg.
- Published
- April 4, 2018
- Distribution
- Wegmans Stores in NY, NJ, PA, VA, MD and…
FDA Recall TerminatedTerminated: August 31, 2020Historical recordClass III
Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA 30062; Manufactured by: Ei LLC, Kannapolis, NC 28083, NDC 61748-220-60.
- Reason
- Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
- Published
- March 28, 2018
- Distribution
- Nationwide
FDA Recall United States TerminatedTerminated: June 3, 2019Historical recordClass III
Ikea North America Srvcs Inc
- Product
- Pink flexible, plastic package: Godis Paskkyckling Marshm…
- Reason
- Possible Pest Contamination at production facility.
- Published
- March 28, 2018
- Distribution
- Nationwide
FDA Recall United States TerminatedTerminated: May 4, 2018Historical recordClass II
Food and Beverage Inc.
- Product
- Name: Trader Joe s Chocolate Chip Cookies SKU 68075 Net Wei…
- Reason
- Food & Beverage Inc., dba Chris's Cookies has initiated a recall of Trader Joe s Peanut Butter Sutter s Formula Cookies (Trader Joes SKU 93307) that was packed in a Trader Joes branded Chocolate Chip Cookie bag, and sent out as Chocolate Chip Cookies. Please note the Chocolate Chip Cookie bag has a statement on the back that says: MAY CONTAIN TRACES OF PEANUTS AND TREE NUTS , but since the wrong product packed is based almost completely in peanut this could represent a bigger risk for those who have peanuts allergies. Thus, prompting the firm to error on the side of public safety and initiate a recall.
- Published
- March 28, 2018
- Distribution
- The product was distributed to the follo…
FDA Recall United States TerminatedTerminated: November 4, 2020Historical recordClass I
WEIS MARKETS
- Product
- Weis Sunbury, PA 17801; Penne W/Asiago Sauce And Grilled Chi…
- Reason
- Penne W/Asiago Sauce and Grilled Chix Small Meal is recalled due to undeclared milk.
- Published
- March 28, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: February 18, 2021Historical recordClass II
Valacyclovir Tablets USP 1 gram, 30-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India NDC # 31722-705-30
- Reason
- Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: February 18, 2021Historical recordClass II
Valganciclovir Tablets, USP, 450 mg, 60-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India. NDC # 31722-832-60
- Reason
- Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: June 8, 2020Historical recordClass III
Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets, USP 5/1.5 mg Rx Only 30 Tablets Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873 Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 NDC 43386-118-03 UPC 343386118038
- Reason
- Failed Impurities/Degradation Specifications
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: April 29, 2019Historical recordClass III
Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Manufactured by: DPT, Laboratories Ltd. San Antonio, TX 78215, NDC 43598-341-90
- Reason
- Failed Stability Specifications:Out-of-specification results observed for viscosity during stability testing.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: August 7, 2019Historical recordClass I
Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Hospira, Inc., Lake forest, IL 60045 USA. NDC: 0409-2634-01
- Reason
- Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: August 7, 2019Historical recordClass I
Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618. NDC: 0703-0110-01
- Reason
- Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: December 2, 2019Historical recordClass II
Sermorelin Acetate, powder, a) 1 GM-bottle (NDC58597-8092-1) b) 5 GM-bottle (NDC 58597-8092-2) c) 10 GM-bottle (NDC 58597-8092-4) API American Pharmaceutical Ingredients
- Reason
- Stability Data Does Not Support Expiry: Stability data from manufacturer does not support expiration dates listed.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: December 2, 2019Historical recordClass II
Oxytocin USP, powder, 1g-bottle, API American Pharmaceutical Ingredients, NDC 58597-7042-3
- Reason
- Stability Data Does Not Support Expiry: Stability data from manufacturer does not support expiration dates listed.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: June 26, 2020Historical recordClass III
Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed by: ALVA-AMCO Pharmacal Cos., Inc., Niles, IL 60714, USA. NDC 52389-745-56, UPC 0 72959 01045 4.
- Reason
- Subpotent Drug: The product has failed to maintain its label claim of coal tar throughout its labeled 24-month expiry period.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: April 15, 2020Historical recordClass II
methylPREDNISolone Sodium Succinate for Injection, USP, 1 gram* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-810-30.
- Reason
- Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: April 15, 2020Historical recordClass II
methylPREDNISolone Sodium Succinate for Injection, USP, 125 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-808-10.
- Reason
- Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: April 15, 2020Historical recordClass II
methylPREDNISolone Sodium Succinate for Injection, USP, 40 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-807-05.
- Reason
- Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
- Published
- March 21, 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.