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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: WA ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 13, 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

phenylephrine 50 mg added to 0.9% sodium chloride 250mL, CONCENTRATION = 200mcg/mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043. NDC:72196-7039-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine, 40mg/250ml, added to 0.9% sodium chloride, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6092-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

phenylephrine, 25mg added to 0.9% sodium chloride 250 mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-7011-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EPINEPHrine, 2 mg added to dextrose 5% 250mL, Concentration = 8 mcg/mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6030-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

vancomycin 1 g/250 mL added to 0.9% sodium chloride, 4 mg/mL, IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-6064-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation or Injection, Must be Diluted, Manufactured by: The Ritedose Corporation Columbia, SC 29203 for Ritedose Pharmaceuticals, LLC Columbia, SC 29203, NDC 76204-025-96.

by The Ritedose Corporation

Reason: CGMP deviation: product released prior to supplier approval.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Eat Good LLC

Product: Mediterranean Salad is a food service refrigerated product,…
Reason: Label declares pepperoncini but does not declare sulfite and FD&C Yellow #5. Label declares feta cheese but does not declare milk.
Published: August 9, 2023
Distribution: Distributed in ID, MT, and WA.

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FDA Recall United States Terminated Historical recordClass II

Eat Good LLC

Product: Mandarin Noodle Salad is a food service refrigerated product…
Reason: Label declares pasta but does not declare wheat.
Published: August 9, 2023
Distribution: Distributed in ID, MT, and WA.

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FDA Recall United States Terminated Historical recordClass II

Eat Good LLC

Product: Greek Orzo Pasta Salad is a food service refrigerated produc…
Reason: Label declares orzo and feta cheese but does not declare orzo pasta (wheat) and Milk.
Published: August 9, 2023
Distribution: Distributed in ID, MT, and WA.

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FDA Recall United States Terminated Historical recordClass II

Eat Good LLC

Product: Elote Corn Salad is a food service refrigerated product, pac…
Reason: Label declares feta cheese but does not declare Milk.
Published: August 9, 2023
Distribution: Distributed in ID, MT, and WA.

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FDA Recall United States Terminated Historical recordClass II

Eat Good LLC

Product: Caesar Pasta Salad is a food service refrigerated product, p…
Reason: Label declares Pasta, Parmesan cheese, Mayonnaise but does not declare Wheat, Milk, and Soybean Oil.
Published: August 9, 2023
Distribution: Distributed in ID, MT, and WA.

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FDA Recall United States Terminated Historical recordClass II

ZB Importing LLC

Product: Ziyad Brand Jameed Soup Starter sold in a 35.2 fluid ounce t…
Reason: Does not declare the major food allergen "milk"
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Plantation Candies, Inc.

Product: Plantation Candies Petite Misty Mints 10 lbs and 25 lb boxes…
Reason: Undeclared soy
Published: August 9, 2023
Distribution: Distributed to consignees in WA, MA, MI,…

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FDA Recall Ongoing Historical recordClass II

Testosterone Cypionate-Testosterone Propionate 180-20 mg/mL in cottonseed oil, Compounded Rx, For Intramuscular Use Only, a) 1 mL, b) 5 mL Multi-Dose Vial, New Vitalis Pharmacy, 4139 Cadillac Ct, Ste 201, Louisville, KY 40213

by New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Reason: Lack of Assurance of Sterility
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Safe Tussin PM Night Time Cough Relief (Cough Suppressant/Antihistamine), packaged in 4.0 FL OZ(118mL) bottles, Kramer Laboratories, Inc. Bridgewater, NJ 08807

by Kramer Laboratories, Inc.

Reason: CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough Suppressant Guaifenesin/Expectorant), packaged in 4.0 FL OZ(118mL), 2020 Kramer Laboratories, Inc. Bridgewater, NJ 08807

by Kramer Laboratories, Inc.

Reason: CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Diclofenac Sodium Topical Solution USP, 2% w/w, 3.8 FL.OZ.(112 grams) bottles, Rx only, Manufactured for: Alembic Pharmaceuticals, Inc. Bedminster, NJ 07921, USA Manufactured by: Alembic Pharmaceuticals Limited (Derma Division) Karakhadi, Vadodara 391450, India. NDC 62332-487-12

by ALEMBIC PHARMACEUTICALS, INC.

Reason: Defective Delivery System
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 57664-230-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Presence of Foreign Substance: Metal embedded in a tablet.
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Oxacillin for Injection, USP, 10 gram per pharmacy Bulk Package bottle, For Intravenous Use, Rx only, packaged as a) NDC 25021-163-99 and b) novaplus NDC 25021-163-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.

by Sagent Pharmaceuticals

Reason: Lack of Assurance of Sterility
Published: August 2, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Oxacillin for Injection, USP, 2 grams per vial, For IV or IM Use, Rx only, labeled as a) NDC 25021-162-24 and b) novaplus NDC 25021-162-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.

by Sagent Pharmaceuticals

Reason: Lack of Assurance of Sterility
Published: August 2, 2023
Distribution: Nationwide

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Data last updated: September 13, 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.