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 1181–1200 of 1639 results

Sort:

Newest first Oldest first

ISOMORPH Whey Isolate Cookies N Cream (Hi Tech) – undeclared allergens (2021)

Undeclared Milk

During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.

FDAApr 3, 2021AL, AZ, AR +41 more• Hi Tech Pharmaceuticals

IMPERIAL GOLD 2000 (QMart) - Undeclared Ingredients (2021)

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Class IIModerate

FDAMar 31, 2021Nationwide• QMart

Imperial Platinum 2000 (QMart) - Undeclared Ingredients (2021)

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Class IIModerate

FDAMar 31, 2021Nationwide• QMart

Guanfacine Tablets (Apotex) - Cross Contamination (2021)

Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate

Class IIModerate

FDAMar 31, 2021Nationwide• Apotex Corp.

PremierZen Extreme 3000 (QMart) - Undeclared Ingredients (2021)

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Class IIModerate

FDAMar 31, 2021Nationwide• QMart

Burro en Primavera (QMart) - Undeclared Ingredients (2021)

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Class IIModerate

FDAMar 31, 2021Nationwide• QMart

Triple SupremeZen Gold (Na Na) - Undeclared Ingredients (2021)

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Class IIModerate

FDAMar 30, 2021Nationwide• Na Na Collection

PremierZen Platinum 5000 (Na Na) - Undeclared Ingredients (2021)

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Class IIModerate

FDAMar 30, 2021Nationwide• Na Na Collection

Thumbs Up 7 Black (Nuri Trading) - Undeclared Ingredients (2021)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil, an FDA approved drug making this an unapproved drug for which the safety and efficacy has not been established and therefore subject to recall.

FDAMar 29, 2021Nationwide• Nuri Trading LLC

Shogun-X 7000 (Nuri Trading) - Undeclared Ingredients (2021)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.

FDAMar 29, 2021Nationwide• Nuri Trading LLC

69MODE Blue 69 (Nuri Trading) - Undeclared Ingredients (2021)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making it an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

FDAMar 29, 2021Nationwide• Nuri Trading LLC

Thumbs Up 7 White (Nuri Trading) - Undeclared Ingredients (2021)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil sildenafil, and vardenafil, FDA approved drugs making them an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

FDAMar 29, 2021Nationwide• Nuri Trading LLC

Imperial Extreme 2000 Capsules (S & B Story) – Unapproved Drug Ingredients (2021)

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.

Class IIModerate

FDAMar 25, 2021Nationwide• S & B Story LLC

Methylprednisolone Tablets (DocRx) – Illegible Label (2021)

Labeling: Illegible label: Manufacturer received complaint of mis-alignment print of the printed dosing instructions on the blister card.

FDAMar 19, 2021AL, CA, IN +1 more• Asclemed USA Inc. dba Enovachem Pharmaceuticals

Evrysdi Prescription Drug (Genentech) – Packaging Issue (2021)

This recall involves bottles of the prescription drug Evrysdi, a prescription medicine used to treat spinal muscular atrophy (SMA) in adults and children 2 months of age and older. The recalled 100 mL amber bottles have "Evrysdi (risdiplam) for oral solution," the dosage and "NDC 20242-175-07" on the front of the bottle labels.

CPSCMar 18, 2021Nationwide• Genentech, a member of the Roche Group, of South San Francisco, Calif.

Imatinib Mesylate Tablets (Dr. Reddy's) – Poisoning Risk (2021)

This recall involves blister packages of prescription medications. The name and strength of the medication, "For Institutional Use only," "Rx Only," lot number and expiration date are printed on the outside of the package as well as on the individual blister units. The Dr. Reddy's logo and NDC number are printed on the outside of the package. The recalled medications include the following: Recalled Prescription Drugs NDC Numbers Carton Configurations Lot Numbers Expiration Dates Imatinib Mesylate Tablets 100 mg 43598-344-31 3 blister cards of 10 tablets H2000138 2022-0630 Imatinib Mesylate Tablets 400 mg 43598-345-31 3 blister cards of 10 tablets H2000127 2022-0630 Pregabalin Capsules 50 mg 43598-292-66 5 blister cards of 10 capsules T900876 2021-0630 Pregabalin Capsules 75 mg 43598-293-66 5 blister cards of 10 capsules T901021 2021-0731 Pregabalin Capsules 100 mg 43598-294-66 5 blister cards of 10 capsules T901022 2021-0731 Pregabalin Capsules 150 mg 43598-295-66 5 blister cards of 10 capsules T901023 2021-0731 Sevelamer Carbonate Tablets 800 mg 55111-789-11 4 blister cards of 25 tablets T801003, T000009, T900221 2020-1031, 2021-1231, 2021-0228 Tadalafil Tablets 5 mg 43598-575-31 3 blister cards of 10 tablets T000376 2022-0131 Tadalafil Tablets 20 mg 43598-573-31 3 blister cards of 10 tablets T000425 2022-0228

CPSCFeb 25, 2021Nationwide• Dr. Reddy's Laboratories, Ltd., of India

Enoxaparin Sodium (Apotex) – labeling mixup (2021)

Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL (corresponding to 100 mg/mL strength) instead of 150 mg/mL (corresponding to 120 mg/0.8mL strength)

FDAFeb 2, 2021Nationwide• Apotex Corp.

Enoxaparin Sodium (Apotex) – labeling mixup (2021)

Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength)

FDAFeb 2, 2021Nationwide• Apotex Corp.

Spironolactone Tablets (Bryant Ranch) – Label Mix-Up (2021)

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.

Class IIModerate

FDAJan 27, 2021Nationwide• Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Spironolactone Tablets (Bryant Ranch) – Label Mix-Up (2021)

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.

FDAJan 27, 2021Nationwide• Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

1...58 596061 62...82

Page 60 of 82Next