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 3881–3900 of 9030 results

Sort:

Newest first Oldest first

Blackberries (Driscoll's) – Pesticide Tolerance Excess (2018)

Random sample indicated an over tolerance for three pesticides: Thidiazuron; forchlorfenuron; and Thiamethoxam.

FDAApr 15, 2018IN, MI, MO +1 more• Driscoll's Strawberry Associates, Inc.

Artichoke Spread (Eataly) – Undeclared Walnuts (2018)

Undeclared Allergen

Product contains undeclared walnuts.

FDAApr 14, 2018NY• EATALY NY, LLC (DUTY ONLY)

Calendula Cream (Boiron) – Incorrect Ingredient Labeling (2018)

Labeling: Labeling Error on Declared Strength; The outer carton (secondary packaging) statement of ingredients misstates the concentration of active ingredient at 7%. The primary packaging (tube) correctly states the active ingredient at 10%.

Class IIILow

FDAApr 13, 2018Nationwide• Boiron Inc.

Hunting Knife (Nextorch) – Laceration Hazard (2018)

Laceration Risk

This recall involves the Allagash fixed blade hunting knife with sheath. The sheath measures 7 inches long by 2 inches wide, is made of brown leather and contains white stitching down one side. The knife blade measures 3.55 inches long by 1 inch wide, is made of stainless steel and is attached to a light brown handle. L.L.Bean is embossed on the brown leather sheath and engraved on the top of the knife blade near handle on one side. The recalled knife with sheath has the product identification number 501794 printed on the green box in which the knife is packaged.

CPSCApr 12, 2018Nationwide• Nextorch Industries Co. LTD, of China

Keta Salmon (Seabear) – Storage Mislabeling (2018)

Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels

FDAApr 11, 2018Nationwide• Seabear Company

Morphine Sulfate Injection (Premier Pharmacy) – Sterility Risk (2018)

Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.

Class IIModerate

FDAApr 11, 2018Nationwide• Premier Pharmacy Labs Inc

NEOstigmine Methylsulfate (Premier Pharmacy) – Sterility Risk (2018)

Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.

Class IIModerate

FDAApr 11, 2018Nationwide• Premier Pharmacy Labs Inc

Morphine Sulfate Injection (Premier Pharmacy) – Sterility Risk (2018)

Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.

Class IIModerate

FDAApr 11, 2018Nationwide• Premier Pharmacy Labs Inc

Hydromorphone HCl Injection (Premier Pharmacy) – Sterility Risk (2018)

Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.

Class IIModerate

FDAApr 11, 2018Nationwide• Premier Pharmacy Labs Inc

Technetium TC-99M Mebrofenin (Pharmalucence) – Failed Stability (2018)

Failed Stability Specifications

Class IIModerate

FDAApr 10, 2018Nationwide• Pharmalucence, Inc.

Re-fuel Power Bank Charging Station (Unknown) – Fire Hazard (2018)

This recall involves the Re-fuel by Digipower Grab and Go Family Pack portable power bank charging stations. The power bank charger is a self-contained energy source used to charge cell phones and other devices when an electrical outlet is not available. The unit consists of three (black, gray and green) 2600 mAh re-chargeable lithium-ion battery chargers that sit on a recharging docking station. Each power bank is oval in shape and measures approximately 3.75 inches long by 1.25 inches high by 0.75 inches wide. "re-fuel by DIGIPOWER" is printed on each power bank. Item number RF-TRIP is printed on the bottom of the charging station.

CPSCApr 5, 2018Nationwide

PAW PATROL Marshall Hat (Rayland) – Fire Hazard (2018)

This recall involves the Nickelodeon PAW PATROL Deluxe Marshall Hat sold with an accessory flashlight. The PAW PATROL Marshall hats are red with a yellow ribbon, black and white spotted dog ears and a black flash light attached to the side of the hat. The flashlight is included with the hat and they share the SKU number. Only flashlights with SKU 01292093 and date codes 1703RY01, 1603RY01, and 1503RY01 are involved in this recall.The SKU number and date codes are on the sewn in label under the ear on the hat.

CPSCApr 5, 2018Nationwide• Rayland Ind. Co., of Hong Kong

Cyclophosphamide (Kroger) – Processing Controls Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

Copaxone (Kroger) – Processing Controls Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

Prolia Syringe (Kroger) – Processing Controls Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

Boost VHC Oral Liquid (Kroger) – Processing Controls Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

Lupron Depot Kit (Kroger Specialty) – Processing Control Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

Revlimid Oral Capsule (Kroger Specialty) – Processing Control Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

Perjeta (Kroger) – Processing Controls Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

Pediasure Vanilla Liquid (Kroger) – Processing Controls Issue (2018)

Lack of Processing Controls.

Class IIModerate

FDAApr 3, 2018AR, FL, IL +2 more• Kroger Specialty Pharmacy, Inc.

1...193 194195196 197...452

Page 195 of 452Next