Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Search Product Recalls

Try:····

Filters

Category

All Categories Food Medication Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Time Period

All Time Last 30 Days Last 90 Days Last Year

State

Severity

All Severities Class I (High Risk)Class II (Moderate)Class III (Low)

Source

All Sources FDA CPSC USDA NHTSA

Status

Include terminated recalls

Clear all filters

Showing 1821–1840 of 3363 results

Sort:

Newest first Oldest first

Montelukast Sodium Granules (Mylan) – Impurity Specification (2017)

Failed Impurities/Degradation Specifications; out of specification results for Sulphoxide Impurity and Total Impurities

FDAMay 9, 2017Nationwide• Mylan Pharmaceuticals Inc.

Benzonatate Capsules (Strides) – Preservative Content Issue (2017)

Failed Stability Specifications: Out of Specification results obtained for preservative Methylparaben content.

FDAMay 9, 2017Nationwide• Strides Pharma INC

Denali Moose Tracks Cheesecake (Father's Table) – labeling error (2017)

Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.

Class IIILow

FDAMay 9, 2017FL, GA, IN• The Father's Table, LLC

Hydrocortisone Lotion (Qualitest) – Superpotent Drug (2017)

Superpotent Drug: above specification for the assay.

FDAMay 8, 2017Nationwide• Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Move Free Advanced Plus (RB Manufacturing) – packaging error (2017)

RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.

FDAMay 8, 2017Nationwide• RB Manufacturing LLC

Amlodipine Besylate Tablets (Ascend) – Tablet Mixup (2017)

PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet was found co-mingled with 10 mg Amlodipine Besylate tablets in a bottle labeled as Amlodipine Besylate 10 mg.

FDAMay 5, 2017Nationwide• Ascend Laboratories LLC

Famotidine Oral Suspension (Lupin) – CGMP Deviation (2017)

CGMP Deviations

FDAMay 2, 2017Nationwide• Lupin Pharmaceuticals Inc.

Protein Bar (Herbalife) – undeclared fish gelatin (2017)

Herbalife is recalling Protein Bar-Peanut Butter because it may contain a trace amount of fish gelatin.

FDAMay 1, 2017Nationwide• Herbalife International Of America Inc

Minivelle Patch (Noven) – Defective Delivery System (2017)

Defective Delivery System: Out of specification for peel force from the release liner specification during stability testing at 18M 25C/60%RH.

FDAApr 27, 2017Nationwide• Noven Pharmaceuticals, Inc.

Acyclovir Tablets (Hetero) – Foreign Substance (2017)

Presence of Foreign Substance: human hair melded into tablet.

FDAApr 27, 2017Nationwide• Hetero USA Inc

Amoxicillin Potassium Tablets (Sandoz) – Subpotent Drug (2017)

Subpotent Drug; Clavulanic Acid

FDAApr 26, 2017NY, OH• Sandoz Inc

IC-Green Injection (Akorn) – Low pH Value (2017)

Product is being recalled due to low pH value.

FDAApr 20, 2017Nationwide• Akorn, Inc.

Children's Cetirizine Tablets (Sun Pharmaceutical) – Specification Failure (2017)

Failed Tablet/Capsule Specifications: out of specification results for increased tablet hardness.

FDAApr 18, 2017Nationwide• Sun Pharmaceutical Industries, Inc.

Zinc Oxide Paste (Fagron) – Labeling Error (2017)

Labeling: Error on Declared Strength: Error is due to an incorrect value in the Drug Facts Panel. The correct strength is displayed on the primary container.

FDAApr 17, 2017Nationwide• Fagron, Inc

Allergy Relief (P & L Development) – Subpotent Product (2017)

Subpotent: This product is being recalled due to low out of specification assay results at the 9 month time point.

FDAApr 17, 2017Nationwide• P & L Development, LLC

Mexican Wedding Cookie (Moondance) – undeclared pecans (2017)

Undeclared Allergen

undeclared pecans

FDAApr 17, 2017CA, FL, GA +6 more• Moondance Heavenly Desserts, LLC

Desoximetasone Ointment (Teligent) – Potency Issue (2017)

Superpotent Drug

FDAApr 7, 2017TN• Teligent, Inc.

Doxercalciferol Capsules (West-Ward) – illegible print (2017)

Failed Tablet/Capsule Specifications; during an internal inspection, capsules were found with illegible print.

FDAApr 4, 2017OH• West-Ward Columbus, Inc.

Dry Figs (Global Commodities) – Undeclared sulfites (2017)

Undeclared Allergen

Presence of Undeclared Sulfites

FDAMar 31, 2017MA, NJ, NY +1 more• GLOBAL COMMODITIES INC

PrednisoLONE Oral Solution (Teva) – stability failure (2017)

Failed Stability Specifications

FDAMar 28, 2017Nationwide• Teva Pharmaceuticals USA

1...90 919293 94...169

Page 92 of 169Next