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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,113
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,781–5,800 of 18,020 recalls

FDA Recall Terminated Historical recordClass II

ESTRADIOL VALERATE 50MG/ML IN ETHYL OLEATE INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall Terminated Historical recordClass II

ESTRADIOL VALERATE 10MG/ML IN ETHYL OLEATE 10MG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

View recall →

FDA Recall Terminated Historical recordClass II

CJC-1295 4MG/IPAMORELIN 4MG VIAL 4MG/4MG INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall Terminated Historical recordClass II

BLUE TREE LIPO EXTREME (/W METHYLCOBALAMIN) INJECTION INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall Terminated Historical recordClass II

B COMPLEX INJ CMP-NO B12, NO LIDOCAINE INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall Terminated Historical recordClass II

ALPROSTADIL 40MCG/ML INJ 40MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall Terminated Historical recordClass II

ALPROSTADIL 22MCG/ML 22MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall Terminated Historical recordClass II

(WELL'S LIPO-LEAN)INOSITOL/CHOLINE/B-COMP+LEUCINE+CARN+ CHROM+LIDO 25MG/25MG/1.5MG/25MG/25MCG/10MG INJECTABLE in vials, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall Terminated Historical recordClass II

Estradiol Valerate 20 mg/mL in Ethyl Oleate Inj. 20 mg/mL Injection in vials, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247

by Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Reason
Lack of assurance of sterility
Published
November 17, 2021
Distribution
United States including Washington, D.C.…

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FDA Recall United States Terminated Historical recordClass I

Simply Delicious, Inc.

Product
Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack,…
Reason
Almond Butter Bars contain undeclared peanuts.
Published
November 17, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01

by MERCK SHARP & DOHME CORP

Reason
Presence of Particulate Matter: Identified as Glass Particles
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Completed Historical recordClass I

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504

by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Reason
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Irbesartan Tablets USP, 300 mg a) 30 count (NDC 68180-412-06) and b) 90 count NDC# 68180-412-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Irbesartan Tablets USP, 150 mg a) 30 count (NDC 68180-411-06) and b) 90 count (NDC 68180-411-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Irbesartan Tablets USP, 75 mg a) 30 count (NDC 68180-410-06) and b) 90 count (NDC 68180-410-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, 500 count bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA NDC 43598-743-05

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in the bottle
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, a) 30 count (NDC 43598-743-30), b) 90 count (NDC 43598-743-90) bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Published
November 10, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/80 mg, a) 30 count (NDC 43598-745-30), b) 90 count (NDC 43598-745-90), and c) 500 count (NDC 43598-745-05) bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Published
November 10, 2021
Distribution
Nationwide

View recall →

Data last updated:

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.