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Recall totals

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

37,449

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 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 7, 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 7, 2023Historical recordClass II

Calcium Chloride Injection, For IM Use, Refrigerate, Shake Well, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0225-3

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Biotin (Vitamin H) Injectable Suspension, BIOTIN 10 MG/ML INJ SUSP, For IM Use, Refrigerate, Shake Well, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0220-3

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [5ML] 7MG/ML INJ SUSP, For IM, IA Use, Shake Well. 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0621-5

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [10ML] 7MG/ML INJ SUSP, For IM, IA Use, Shake Well, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0621-1

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [2ML] 6MG/ML INJ SUSP, For IM, IA, IT Use, Shake Well. Preservative Free. Discard Unused Portion, 2 mL Single-use Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0620-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

B-COMPLEX 110 INJECTABLE, For IV, IM, SC Use, Refrigerate, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0212-3

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

AscorbiX (Buffered C) Injection, Ascorbix (50ML) 500MG/ML Injectable, For IV, IM, SC Use, Refrigerate, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0226-5

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

AscorbiX (Buffered C) Injection, Ascorbix (30ML) 500MG/ML Injectable, For IV, IM, SC Use, Refrigerate, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0226-3

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate Injection 40MCG/30MG/2MG/ML Injectable, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0546-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate Injection 20MCG/30MG/1MG/ML Injectable, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0545-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Alprostadil (prostaglandin E1) 80 MCG/ML Injectable, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0543-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Alprostadil (prostaglandin E1)150 MCG/ML Injectable, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0538-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate/Atropine Sulfate Injection, 60 mcg/30 mg/2 mg/0.15mg/ml, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0550-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate/Atropine Sulfate Injection, 40 mcg/25 mg/0.5mg/0.01mg/ml, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0549-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 7, 2023Historical recordClass II

Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate/Atropine Sulfate Injection, 18 mcg/1.8mg/0.2mg/0.02mg/mL, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0547-2

by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Reason: Lack of Assurance of Sterility
Published: March 11, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 6, 2020Historical recordClass II

Mesalamine Delayed-Release Tablets, USP, 1.2 gram, 120-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 0591-2245-22.

by Teva Pharmaceuticals USA

Reason: Failed Dissolution Specifications: Low out of specification dissolution result observed during stability testing.
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I

Choice Products LLC.

Product: Premiere Choice 3lb. Peanut Butter Cookie Dough, item 412, N…
Reason: Peanut Butter Cookie Dough may contain undeclared milk.
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 24, 2020Historical recordClass III

Custom Foods LLC

Product: Sticky Fingers Bakeries Gluten-Free Scones, Quick & Easy Mix…
Reason: Firm received customer inquiry of why wheat is listed in the ingredient list of a product that is "Gluten Free".
Published: March 11, 2020
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 13, 2020Historical recordClass II

Michele's Granola LLC

Product: Michele s Granola, MOM s Salted Maple Pecan Granola, 4 Cases…
Reason: Michele's Granola LLC. has initiated a recall of MOM s Salted Maple Pecan Granola, because of incorrectly labelled bags. (The incorrect back label with ingredient list does not list pecans as an ingredient.) Lot Number: 8/14/2020 , Best By date: 8/14/2020 .
Published: March 11, 2020
Distribution: The product was distributed to one retai…

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FDA Recall United States TerminatedTerminated: March 3, 2020Historical recordClass III

Driscoll's Inc.

Product: Driscoll's Raspberries- 6 oz. clamshell container 12 x 6 oz…
Reason: In House testing found a residue of 0.927 ppm of Zeta-cypermethrin on raspberries, which is above the U.S. MRL of 0.800 ppm
Published: March 11, 2020
Distribution: PA, KY, MA, MI. MD, FL, CO, MI, NC, NJ,…

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Data last updated: November 7, 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.