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Recall totals

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

37,140

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 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 25, 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

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

fentaNYL Citrate Injection, 50 mcg per mL, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3153.

by PharMEDium Services, LLC

Reason: Subpotent Drug and Stability Data Does Not Support Expiry: confirmed subpotency and potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL Citrate Injection, 50 mcg per mL, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Product code 2R3118, NDC 61553-118-40

by PharMEDium Services, LLC

Reason: Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Fentanyl Citrate 16.67 mcg per mL and Bupivacaine HCl 0.1667% in 0.9% Sodium Chloride, Total Dose 25.005 mcg/1.5 mL Fentanyl Citrate, Content Volume 1.5 mL in 3 mL BD Syringe, Intended for Epidural Use, Rx only, PharMEDium, Product code 2T6228.

by PharMEDium Services, LLC

Reason: Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3308.

by PharMEDium Services, LLC

Reason: Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, 5 mg per mL, 25 mg per 5 mL, in 0.9% Sodium Chloride, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3301.

by PharMEDium Services, LLC

Reason: Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Buffered Lidocaine, 2%, In Sodium Bicarbonate 8.4%, 3 mL Total Volume in a syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2475.

by PharMEDium Services, LLC

Reason: Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2466.

by PharMEDium Services, LLC

Reason: Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

atropine Sulfate Injection, 0.4 mg per mL, 0.8 mg per 2 mL, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3335.

by PharMEDium Services, LLC

Reason: Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amikacin Sulfate Injection, USP, 500 mg/2 mL (250 mg/mL) Rx Only, Manufactured in Hungary For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-9032-01 (individual pack), NDC 0703-9032-03 (shelf-pack carton of 10 vials).

by Teva Pharmaceuticals USA

Reason: CGMP Deviations
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative, One Pint (473 mL) bottles, Dist by: Rugby Laboratories, Livonia, MI --- NDC 0536-0590-85

by The Harvard Drug Group

Reason: Microbial contamination of Non-Sterile Products; positive findings of Burkholderia cepacia
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vancomycin 10 mg/mL in 0.9% Sodium Chloride (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-005-35

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Placebo for Prednisolone Acetate 1%, Oph Suspension, 10 mL Dropper Bottle, Compounded by Leiter's Compounding, San Jose, CA

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Moxifloxacin 1 mg/mL in Sterile Balanced Salt Solution (BSS) Intravitreal Injection, 1 mL Total Volume in a 2 mL Vial, Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-003-35

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Mitomycin 0.02% (0.2 mg/mL) in Sterile Water for Injection (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-005-35

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lidocaine HCl 1% - Phenylephrine HCl 1.5% in Sterile Water for Injection (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-002-35

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cyclopentolate HCl 1% - Tropicamide 1% - PHENYLephrine HCl 2.5% in Sterile Water for Injection (Ophthalmic Solution), in a) 1 mL Total Volume (NDC 70360-017-38) and b) 10 mL Total Volume (NDC 70360-017-39) in a 15 mL Dropper Bottle, Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-017-38

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cefuroxime Sodium 10 mg/mL in 0.9% Sodium Chloride (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-007-35

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Brilliant Blue G 0.025% in 0.9% Sodium Chloride (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-008-35

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Atropine Sulfate 0.01% in 0.9% Sodium Chloride (Ophthalmic Solution) 10 mL Total Volume in a 15 mL Dropper Bottle, Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-011-39

by Leiter's Compounding

Reason: Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Published: October 19, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Paricalcitol Capsules, 1 mcg, packaged in 30 Capsules (5 x 6) per carton (NDC 60687-106-25); each blister card containing 6 individually blistered capsules (NDC 60687-106-95), Rx only, Distributed by: American Health Packaging, Columbus, OH, 43217.

by Amerisource Health Services

Reason: Failed Impurities/Degradation Specifications: This repackaged product was recalled by its manufacturer due to failed results for impurities.
Published: October 19, 2016
Distribution: Nationwide

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Data last updated: September 25, 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.