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Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 20, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass II

Oxacillin for Injection, USP, 2 grams per vial, For IV or IM Use, Rx only, labeled as a) NDC 25021-162-24 and b) novaplus NDC 25021-162-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.

by Sagent Pharmaceuticals

Reason: Lack of Assurance of Sterility
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Oxacillin for Injection, USP, 1 gram per vial, For IV or IM Use, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India. NDC 25021-146-10.

by Sagent Pharmaceuticals

Reason: Lack of Assurance of Sterility
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 17, 2024Historical recordClass II

Famotidine Tablets, USP, 20mg, 200-count bottle within a carton, Distributed by: Glenmark Therapeutics Inc., USA, Mahwah, NJ 07430, Made in India, NDC 72657-113-20.

by Glenmark Therapeutics, Inc.

Reason: Labeling: Label Error on Declared Strength: some cartons labeled and containing 20 mg may have an external label placed on the side of the carton indicating strength as 10 mg.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 8, 2024Historical recordClass II

Norepinephrine 32 mg per 250 mL (128 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per case, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-702-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 8, 2024Historical recordClass II

Norepinephrine 16 mg per 250 mL (64 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per carton, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-602-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 8, 2024Historical recordClass II

Norepinephrine 8 mg per 250 mL (32 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per case, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-577-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 8, 2024Historical recordClass II

Norepinephrine 4 mg per 250 mL (16 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per case, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-552-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 8, 2024Historical recordClass II

Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL Single Dose bag, packaged in 1000 mL x 6 units per case, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-326-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 4, 2023Historical recordClass II

Vancomycin HCl 1.5 g added to 0.9% Sodium Chloride 500 mL, 500 mL IV Bag (515 total volume), Rx Only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042, NDC 71546-310-50;

by New England Life Care, Inc. dba Advanced Compounding Solutions

Reason: CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 4, 2023Historical recordClass II

ROcuronium Bromide 50 mg/5 mL ( 10 mg/mL), 5mL Syringe, RX Only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042, NDC: 71546-090-05

by New England Life Care, Inc. dba Advanced Compounding Solutions

Reason: CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 4, 2023Historical recordClass II

PHENYLephrine HCl 10mg added to 0.9% Sodium Chloride 250mL, 250 mL IV Bag @60 Total volume), RX only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042, NDC: 71546-450-25;

by New England Life Care, Inc. dba Advanced Compounding Solutions

Reason: CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 4, 2023Historical recordClass II

SUCCINYLcholine Chloride 200 mg/10mL (20 mg/mL), 10 mL BD Syringe, Rx Only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042; NDC: 71546-083-10

by New England Life Care, Inc. dba Advanced Compounding Solutions

Reason: CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Fingolimod Capsules, 0.5 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-476-30.

by Ascend Laboratories, LLC

Reason: Failed Dissolution Specifications
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 26, 2024Historical recordClass III

Loteprednol Etabonate Ophthalmic Suspension, 5 mg/mL (0.5%), packaged as one bottle in a carton in a) 10 mL bottle (NDC# 62756-232-55) and b) 15 mL bottle (NDC # 62756-232-56), Rx only, Distributed by: Sun Pharmaceutical Ind., Inc., NJ 08512, Manufactured by: Sun Pharmaceutical Medicare Ltd., India.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Superpotent Drug: Out of Specification (OOS) results observed for unit dose content.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Srikakulam - 532 409 India. NDC 55111-180-10

by Dr Reddy's Laboratories Limited

Reason: Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass I

Braga Fresh Foods

Product: 365 by Whole Foods Market Organic Asian Inspired Chopped Sal…
Reason: Undeclared milk and egg
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 7, 2024Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Seasons Choice Mixed Fruit, Strawberries, Pinneapple, Peache…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 7, 2024Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Seasons Choice Tropical Blend, Pineapple, Mango, Strawberrie…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 7, 2024Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Good & Gather Mixed Fruit Blend Pineapple Chunks, Sliced St…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 7, 2024Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Trader Joe's Organic Tropical Fruit Blend, Pineapple, Banana…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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Data last updated: October 20, 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.