Data Explorer

Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

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 Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

State: NJ ×
Clear all

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.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated September 27, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

Download CSV

Recalls by class
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 II

Trader Joes Company

Product: Trader Joe's Artisan Bread - Organic French Baguette; (Bro…
Reason: FDA was notified by the Canadian Food Inspection Agency of that two lot codes of Trader Joe's Organic French Baguette may be contaminated with Listeria monocytogenes.
Published: June 13, 2018
Distribution: Distribution Centers in CA and PA - reta…

View recall →

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…

View recall →

FDA Recall United States Terminated Historical recordClass II

Ahold Usa

Product: Broccoli cuts, All Natural, No Preservatives, Net Wt 16 OZ;…
Reason: Ahold Delhaize received a report from State of CT of finding significant amount of Listeria monocytogenes in a bag of Stop and Shop's Broccoli Cuts, 16 oz.
Published: June 13, 2018
Distribution: CT, DC, MD, MA, NJ, NY PA, RI, VA and WV

View recall →

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

by Shoreside Enterprises Inc.

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

View recall →

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

by Shoreside Enterprises Inc.

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

View recall →

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…

View recall →

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.

by Lupin Pharmaceuticals Inc.

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

View recall →

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.

by Lupin Pharmaceuticals Inc.

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

View recall →

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.

by Ideaz Llc

Reason: CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.
Published: May 30, 2018
Distribution: Nationwide

View recall →

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.

by Exela Pharma Sciences LLC

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

View recall →

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.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

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

View recall →

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

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

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

View recall →

FDA Recall Terminated Historical recordClass I

Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack, Distributed by AMA Wholesale Inc. Chino Hills, CA, 91709-2618, UPC Code: 718122071128

by AMA Wholesale

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared tadalafil. The presence of tadalafil makes Rhino Extreme 50000 an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Published: May 30, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

screamin' hot (capsaicin) Pain Relieving Gel, 0.03%, packaged in a) 2 OZ (57g) tubes, UPC 7 50263 80072 4; b) 5 oz. (141g) tubes, UPC 7 50263 80007 6; and c) 16 oz. (454g) bottles, UPC 7 50263 80076 2; MFD FOR: Toast Products, 400 Sproul Street, Pittsburgh, PA 15136; NDC 52099-8005.

by Ideaz Llc

Reason: CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.
Published: May 30, 2018
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Nature's Only Choice

Product: Nature's Only Choice B17 BITTER RAW APRICOT EXTRACT AMYGDALI…
Reason: The Vitamin B17 containing product is considered to be a prescription drug, new drug, and unapproved new drug.
Published: May 30, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Piperacillin and Tazobactam for Injection, USP 3.375 grams per vial, For Intravenous Use Only, Single-Dose vial, Rx Only, Manufactured for: AuroMedics Pharma LLC, 6 Wheeling Road, Dayton, NJ 05610. NDC 55150-120-30

by AuroMedics Pharma LLC

Reason: Presence of Particulate Matter: confirmed customer report for presence of visible particulate matter, confirmed as glass
Published: May 23, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Piperacillin and Tazobactam for Injection, USP 4.5 gram/vial* 10-count Single Use Vials per carton, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd. Irungattukottai-602 105, India Mfg. for: Apotex Corp. Weston, FL 33326. NDC 60505-0688-4

by Apotex Inc.

Reason: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency
Published: May 23, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Piperacillin and Tazobactam for Injection, USP 3.375 gram/vial* 10-count Single Use Vials per carton, Rx Only, Mfg. by: Hospira Healthcare India Pvt. Ltd. Irungattukottai-602 105, India Mfg. for: Apotex Corp. Weston, FL 33326. NDC 60505-0687-4

by Apotex Inc.

Reason: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency
Published: May 23, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Riomet (metformin hydrochloride oral solution), 500 mg/5 mL (16 fl. oz.), 473 mL plastic bottle, Manufactured by: Mikart, Inc., Atlanta, GA 30318, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512. NDC 10631-206-02

by Sun Pharmaceutical Industries, Inc.

Reason: Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this recall in response to identified labeling discrepancies in the patient literature.
Published: May 23, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Hydrocortisone Ointment, USP 2.5%, Net Wt. 20g, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed by Perrigo, Allegan MI 49010, NDC 45802-014-02

by Perrigo New York

Reason: Failed Stability Specifications
Published: May 23, 2018
Distribution: Nationwide

View recall →

Data last updated: September 27, 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.