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Recall totals

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

37,448

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/snack-right-super-foods-inc-dba-brads-raw-chips-recalls-brads-crunchy-kale-veggie-chips-duePublished November 2, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 4, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

dilTIAZem HCl in 5% Dextrose Injection, 125 mg per 125 mL, (32 mcg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-951-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

NOREPINEPHRINE in 5% Dextrose Injection, 8 mg per 250 mL (32 mg per mL) Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-476-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

Morphine Sulfate in 5% Dextrose Injection, 100 mg per 100 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-452-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

Midazolam in 0.9% Sodium Chloride Injection, 100 mg per 100 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-102-02.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

EPINEPHrine in 0.9% Sodium Chloride Injection, 16 mg per 250 mL (64 mcg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-627-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

EPINEPHIrine in 0.9% Sodium Chloride Injection, 8 mg per 250 mL (32 mcg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-077-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

EPINEPHIrine in 0.9% Sodium Chloride Injection, 5 mg per 250 mL (20 mcg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-052-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

EPINEPHIrine in 0.9% Sodium Chloride Injection, 4 mg per 250 mL (16 mcg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-227-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

Succinylcholine Chloride Injection, 200 mg per 10 mL (20 mg per mL), 1,000 mL, Rx only, SterRx, 141 Idaho Avenue, Plattsburgh, NY 12903, NDC 70324-826-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1000 mL (12.6 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-326-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

PHENYLepherine HCL in 0.9% Sodium Chloride, 20 mg per 250 mL (80 mcg per mL), Rx only, SterRx, 141 Idaho Avenue, Plattsburgh, NY 12903, NDC 70324-701-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

EPINEPHrine, 2 mg per 250 mL (8 mcg per mL) in 0.9% Sodium Chloride Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY, 12903, NDC 70324-027-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

NOREPINEPHRINE 4 mg per 250 mL (16 mcg per mL) in 5% Dextrose Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-451-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

dilTIAZem HCl 125 mg per 125 mL (1 mg per mL) in 0.7% Sodium Chloride Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY, 12903, NDC 70324-976-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

Morphine Sulfate in 0.9% Sodium Chloride Injection, 100 mg per 100 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Avenue, Plattsburgh, NY, 12903, NDC 70324-427-02.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 6, 2023Historical recordClass II

Midazolam in 0.9% Sodium Chloride Injection, 50 mg per 50 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Ave. Plattsburgh, NY 12003, NDC #70324-102-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 25, 2022Historical recordClass I

Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, NDC 61958-2901-2

by Gilead Sciences, Inc.

Reason: Presence of Particulate Matter: investigation into a customer complaint confirmed the presence of glass particulates.
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 16, 2024Historical recordClass II

Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29

by Teligent Pharma, Inc.

Reason: Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-997-64

by Teligent Pharma, Inc.

Reason: Superpotent Drug: Minimally superpotent
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-997-64

by Teligent Pharma, Inc.

Reason: Superpotent Drug
Published: January 5, 2022
Distribution: Nationwide

View recall →

Data last updated: November 4, 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.