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Recall totals

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

37,450
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresh-ready-foods-llc-recalls-fresh-you-brand-sausage-egg-cheese-biscuit-sandwich-due-possiblePublished November 8, 2026
Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (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
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 14,621–14,640 of 21,307 recalls

FDA Recall United States CompletedHistorical recordClass II

Pinnacle Foods, LLC

Product
AUNT JEMIMA(R) LIL' GRIDDLES(TM) BLUEBERRY MINI PANCAKES, 40…
Reason
Potential for Listeria monocytogenes contamination
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Pinnacle Foods, LLC

Product
AUNT JEMIMA(R) MiNi pancakes, MAPLE BLAST, NET WT 3.2 OZ, UP…
Reason
Potential for Listeria monocytogenes contamination
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Pinnacle Foods, LLC

Product
AUNT JEMIMA(R) 14 BLUEBERRY WAFFLES, NET WT 17.18oz UPC 0196…
Reason
Potential for Listeria monocytogenes contamination
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 15, 2018Historical recordClass II

Saphris 10 mg (asenapine) sublingual tablets, 6x10 count blister packs, Rx only, Black Cherry Flavor, Manufactured by: Catalent UK Swindon, Zydis Ltd, Blagrove, Swindon, Wilshire SN5 BRU, UK Distributed by Forest Pharmaceuticals, Inc. subsidiary of Forest Laboratories, LLC, Cincinnati OH 45209 USA --- NDC 0456-2410-60; Shellpack containing 1 blister card --- NDC 0456-2410-06

by Forest Laboratories, LLC

Reason
Labeling; Label Mixup; blister lidding foil and shell-pack labeled as 10 mg but package actually contains 5 mg tablets
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

PHENYLephrine HCL in 0.9% Sodium Chloride injectable, 10 mg (Final Concentration = 0.1 mg per mL) Total Volume 100 mL, Single Dose Container bag, Preservative Free (Contains Sulfites), Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0810-32

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable, 4g, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0737-32

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 3g, Total Approximate Volume 115 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0524-32

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 2g, Total Approximate Volume 100 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0522-32

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

HYDROmorphone HCL in 0.9% Sodium Chloride injectable, 0.2 mg per ml, Total Volume 100mL, Single Dose Container bag, (Total HYDROmorphone Dose 20 mg per 100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0300-55

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable,20 mcg per mL, Single Dose Container bag, (Total fentanyl Dose 2,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-203-32

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0202-32

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0229-32

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100 mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-55

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 29, 2018Historical recordClass II

morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-32.

by SCA Pharmaceuticals

Reason
Lack of assurance of sterility: Product bags leaking at seam.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: January 13, 2020Historical recordClass III

Nystatin Oral Suspension, USP, 100,000 units/mL, packaged in a) 2 fl.oz. (60mL) bottles (NDC 66689-008-02), and 500,000 units/5mL individual unit dose cup (NDC 66689-037-01) packaged in b) 50 count unit dose cups/case (NDC 66689-037-50) and c) 100 count unit dose cups/case (NDC 66689-037-99) Rx only, Manufactured by: VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason
Failed Impurities/Degradation Specifications: Presence of an impurity peak that exceeds approved specification.
Published
June 7, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: June 9, 2017Historical recordClass II

Northern Fisheries Ltd.

Product
Tuna King Tuna Steaks 10 oz.. ,10 lb Box. Frozen UPC Codes:…
Reason
Histamine Levels above 50ppm
Published
June 7, 2017
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: October 15, 2026Historical recordClass II

Lyrical Foods Inc

Product
Kite Hill Mushroom and Ricotta Ravioli; frozen Ravioli made…
Reason
Ingredient statement for Lyrical Foods Mushroom and Ricotta Flavor Ravioli does not include the ingredient of garlic.
Published
June 7, 2017
Distribution
US only to distributors in MD, MA, CA, F…

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FDA Recall TerminatedTerminated: November 3, 2021Historical recordClass I

LaBri's Body Health Atomic, 60 capsules

by Envy Me

Reason
Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.
Published
May 31, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 16, 2018Historical recordClass II

Shield and Protect Moisture Barrier Cream, 1.1% Clotrimazole, Net Weight 4 oz - 115 g Anti-Fungal, Gentell, Inc., Bristol, PA NDC 61554-232-40

by Gentell, Inc

Reason
GMP Deviations; product may not meet cGMP requirements
Published
May 31, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 26, 2017Historical recordClass I

Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS (0.0000000000003% alkaloids, calculated), Calcarea Phosphorica 6X HPUS, Chamomilla 6X HPUS, Coffea Cruda 6X HPUS, Magnesia Phosphorica 6X HPUS, Rheum 6X HPUS, Silicea 12X HPUS] Quick-Dissolving Tablets, 135-count bottle, Manufactured for: Hyland's, Inc., Los Angesles, CA 90061, NDC 54973-3197-1, UPC 3 54973 31971 4.

by Standard Homeopathic Company

Reason
Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.
Published
May 31, 2017
Distribution
Nationwide

View recall →

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.

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