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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

Class III recallsNot likely to cause adverse health consequences

Quick 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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

State: NJ ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 12, 2026 ET

Summary (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

Recalls by class

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical recordClass I

Methocarbamol Injection, USP 1000mg/10mL, (100mg/mL), 10 mL Single-Dose Vial packed 25 vials per carton, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor, NJ 08520, NDC 55150-223-10

by Eugia US LLC

Reason: Presence of Particulate Matter
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054. Blister Pack NDC 0591-2436-45, Carton NDC 0591-2436-15

by Teva Pharmaceuticals USA, Inc

Reason: Superpotent Drug: The 3-month stability result for assay was found to be above specification limit
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41

by NATCO Pharma Limited

Reason: CGMP Deviations
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India, NDC 6818-0659-06

by Lupin Pharmaceuticals Inc.

Reason: Subpotent Drug
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lidl US TRADING

Product: Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g…
Reason: Undeclared Wheat, Soy, Egg, Milk, Tree Nuts (foreign language labeling)
Published: April 17, 2024
Distribution: Imported product directly shipped to a w…

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FDA Recall United States Terminated Historical recordClass I

Backstage Center DBA CTC Seller

Product: Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35…
Reason: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Coastal Companies DBA Hearn Kirkwood

Product: Egg salad sandwich packaged in clamshell for individual sale…
Reason: Tuna salad sandwich was mislabeled as an egg salad sandwich. There is an undeclared allergen of fish (Tuna).
Published: April 17, 2024
Distribution: Product was sold to institutions, hospit…

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FDA Recall United States Terminated Historical recordClass II

Whitley Peanut Factory, Inc.

Product: Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Elect…
Reason: Undeclared Allergen (peanuts, milk, soy, wheat, and sesame).
Published: April 17, 2024
Distribution: The recalled product was distributed to…

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FDA Recall United States Terminated Historical recordClass II

RAJA FOODS LLC

Product: SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC…
Reason: Product tested positive for lead
Published: April 17, 2024
Distribution: NY, NJ, PA, MD, VA, CT, MA, NH, TN, FL,…

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FDA Recall United States Terminated Historical recordClass III

Nicomex Inc.

Product: Nicomex Tequesquite, Net Wt. 1.5oz (42.52gms), UPC: 8 846781…
Reason: Elevated lead levels
Published: April 17, 2024
Distribution: Distributed to distributors in NJ, then…

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FDA Recall Terminated Historical recordClass III

Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After Reconstitution: For direct intravenous injection or must be further diluted before intravenous infusion, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc., Big Flats, NY 14814, NDC # 39822-0255-01.

by X-Gen Pharmaceuticals Inc.

Reason: Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.
Published: April 10, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Cyclophosphamide for Injection, USP, 500mg/vial, Lyophilized, Cytotoxic Agent, Single Dose Vial for Intravenous Use, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc. Big Flats, NY 14814, NDC # 39822-0250-01.

by X-Gen Pharmaceuticals Inc.

Reason: Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.
Published: April 10, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

fentaNYL Citrate 2,500 mcg/50mL in Sterile Water, 50 mL CADD for Injection, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-6030-1

by IntegraDose Compounding Services LLC

Reason: Lack of Assurance of Sterility: leaking bags
Published: April 10, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00

by B. Braun Medical Inc

Reason: Lack of assurance of sterility: bags have the potential to leak..
Published: April 10, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ, 07430, Product of India, NDC 68462-562-01

by Glenmark Pharmaceuticals Inc., USA

Reason: Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.
Published: April 10, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Turkana Food Inc.

Product: Sekeroglu Lokum Love Turkish Delight With Pistachio And Pome…
Reason: Product contains Acid Red 18
Published: April 10, 2024
Distribution: Distributed to retail stores in CA, CT,…

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FDA Recall United States Terminated Historical recordClass II

Turkana Food Inc.

Product: Sekeroglu Lokum Love Turkish Delight Mixed With Pistachio An…
Reason: Product contains Acid Red 18
Published: April 10, 2024
Distribution: Distributed to retail stores in CA, CT,…

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FDA Recall United States Terminated Historical recordClass II

Waiakea Bottling Inc

Product: Waiakea Hawaiian Volcanic Water Naturally Alkaline Electrol…
Reason: Consumer complaints involving floating particles.
Published: April 10, 2024
Distribution: U.S. distribution to the following: PA,…

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FDA Recall United States Terminated Historical recordClass II

AJI MORI SAUCE CORP

Product: AJI MORI***CHILLIMAMI SAUCE***UMAMI BOMB***NET WT. 250ml. Pa…
Reason: Potential contamination with Clostridium botulinum
Published: April 10, 2024
Distribution: Products were distributed direct to cons…

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FDA Recall Ongoing Historical recordClass I

Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-206-01

by Par Sterile Products LLC

Reason: Presence of Particulate Matter.
Published: April 3, 2024
Distribution: Nationwide

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Data last updated: September 12, 2026 ET

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.