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Recall totals

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

37,115

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 17, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Lyophilized Human Chorionic Gonadotropin 5,500 USP Units For injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910

by Innoveix Pharmaceuticals Inc

Reason: Lack of Sterility Assurance.
Published: November 6, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol Vaginal Inserts USP, 10 mcg, packaged in a) 8-count Vaginal Inserts (with disposable applicators) per carton (NDC 68462-711-71) and b) 18-count Vaginal Inserts (with disposable applicators) per carton (NDC 68462-711-88), Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd., Colvale-Bardez, Goa 403 513, India; Manufactured for: Glenmark Pharmaceuticals Inc., Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective Delivery System: complaints for difficulty in pushing the plunger of the applicator.
Published: November 6, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Prasugrel Tablets 5 mg, 30-count bottles, Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A, NDC 0378-5185-93

by Mylan Pharmaceuticals Inc.

Reason: Failed Dissolution Specification: Low out of specification dissolution results.
Published: November 6, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-filled syringes, Nephron 503B Outsourcing Facility 4500 12th St. Ext West Columbia, SC 29172, NDC 69374-919-10.

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason: Incorrect labeling: Incorrect or missing lot and/or exp date
Published: November 6, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20

by Avella of Deer Valley, Inc. Store 38

Reason: Lack of sterility assurance.
Published: October 30, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-984-10

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason: Lack of Assurance of Sterility; bags have potential to leak
Published: October 30, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl; 25 g L-Lysine HCl, Single Dose Container, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-988-10

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason: Lack of Assurance of Sterility; bags have potential to leak
Published: October 30, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Sodium Chloride Injection-200 mL Total Dose: (400 mcg/200 mg)/200 mL, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-526-20

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason: GMP Deviations: potential glass contamination
Published: October 30, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride Injection-250 mL, Rx Only Total Dose: (500 mcg/312.5 mg)/250 mL, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-530-25

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason: GMP Deviations: potential glass contamination
Published: October 30, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Sodium Chloride Injection-250 mL Total Dose: (500 mcg/156.3 mg)/250 mL, Rx Only, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC 69374-0525-25

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason: GMP Deviations: potential glass contamination
Published: October 30, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Truck Farm, LLC

Product: Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix.…
Reason: The product contains wheat flour, but does not declare wheat on the label.
Published: October 30, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose Vial NDC 50742-464-50 Rx Only Ingenus Pharmaceuticals, LLC. Orlando, FL 32839

by Ingenus Pharmaceuticals Llc

Reason: Crystallization: Presence of particulate matter identified as API crystallization
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Dextroamphetamine Sacharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, Mixed Salts of a single Entity Amphetamine Product), 20mg, 100-count bottle, RX Only, Distributed by: Aurobindo Pharma USA Inc., Dayton, NJ 08810, NDC 13107-073-01

by Aurobindo Pharma USA Inc.

Reason: Superpotent Drug: Amphetamine Mixed Salts 20mg have been found to be out of specification for weight and thickness.
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.

by KVK-Tech, Inc.

Reason: Presence of Foreign Substance; Fiber particles.
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product: Market Sandwich Artisan Style Albacore Tuna Salad on Dark Wh…
Reason: Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product: Tuna Salad on Wheat Bread, Keep Refrigerated. packaged un…
Reason: Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product: Deli Express Tuna Salad on Cracked Wheat Bread, Net Wt 5.0 o…
Reason: Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product: archer farms Turkey & Havarti sandwich on wheat bread Net W…
Reason: Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product: Market Sandwich Ranch chicken Salad on a Croissant. Net Wt.…
Reason: Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published: October 23, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product: Market Sandwich Everything Bagel with Smoked Ham, Smoked Whi…
Reason: Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published: October 23, 2019
Distribution: Nationwide

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Data last updated: September 17, 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.