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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 14, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP 500 mg per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-085-02

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP, 250 mg per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-084-02

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP 10 g per Pharmacy Bulk Package, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-224-15

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP 1g per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-222-41

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP 500 mg per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-221-41

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP 250 mg per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-220-41

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Heparin Sodium, 25,000 USP units per 250mL, (100 USP units per mL) in 5% Dextrose injection, 250 ml Excel Container, B. Braun Medical Inc. Bethlehem, PA 18018, USA; API from Spain NDC: 0264-9587-20,

by B. Braun Medical Inc

Reason: Subpotent: Low anti-factor IIa Potency.
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lorazepam Injection, USP, 2mg/mL, 1 mL vial (NDC 0641-6044-01), packaged in 25 x 1 mL Vials per carton (NDC 0641-6044-25), Rx only, Manufactured by West-Ward, Eatontown, NJ 07724.

by Hikma Pharmaceuticals USA Inc.

Reason: Failed Impurities/Degradation Specifications: Out-of-specification results for total related compounds observed during retain steting due to the elevated Related Compound-C.
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

VANComycin 1.5g added to 250 mL of 0.9% Sodium Chloride Injection, Rx only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-184-25

by Apollo Care, LLC

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Missouri only

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FDA Recall Ongoing Historical recordClass II

FentaNYL 500 mcg (2mcg/mL) and Ropivacaine HCL 250 mg (0.1%) added to 250 mL 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-950-25

by Apollo Care, LLC

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Missouri only

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FDA Recall Ongoing Historical recordClass II

VANComycin 750mg added to 250 mL of 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-255-25

by Apollo Care, LLC

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Missouri only

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FDA Recall Ongoing Historical recordClass II

Norepinephrine 4 mg added to 250 mL of 5% Dextrose Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-500-25

by Apollo Care, LLC

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Missouri only

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FDA Recall Ongoing Historical recordClass II

VANComycin 1.25g added to 250 mL of 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-264-25

by Apollo Care, LLC

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Missouri only

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FDA Recall Ongoing Historical recordClass II

VANComycin 1.25g added to 250 mL of 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-284-25

by Apollo Care, LLC

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Missouri only

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FDA Recall Ongoing Historical recordClass II

Ketamine Injection, 50 mg per 5 mL (10 mg/mL), Single-Use Syringe, Rx only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-050-05

by Apollo Care, LLC

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Missouri only

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FDA Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 4.5 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-080-02

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP 2.25 g per vial,s Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-078-02

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 3.375 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-217-41

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 2.25 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC66794-216-41

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP 4.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-004-51

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

View recall →

Data last updated: September 14, 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.