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 23181–23200 of 29086 results

Sort:

Newest first Oldest first

Original Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari," Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Oil Free Original Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Array LaserLink (Lumenis) – Erroneous Pattern Display (2014)

Lumenis initiated a field-correction for the Array Laser Link", GA-0006700 (SN XXYYZZ) because the system may project an erroneous pattern display on the retina, which is different than the desired pattern.

Class IIModerate

FDAAug 15, 2014Nationwide• Lumenis, Inc.

LAP-BAND AP System (Apollo) – Expired Product Distribution (2014)

Product was distributed past its expiration date.

Class IIModerate

FDAAug 15, 2014CA, DE, IN +4 more• Apollo Endosurgery Inc

Black Bean Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Spinach Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Roasted Red Pepper Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Roots Roasted Garlic Hummus (Roots Organic) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

SELEC-3 I.V. Set (Biomedix) – Product Failure (2014)

Customer contacted Biomedix of complaint and returned the failed set along with 86 units of unopened stock (96 units originally shipped). Biomedix performed extensive investigation and found insufficient application of glue. Recall was initiated due to the rate of the failure.

Class IIModerate

FDAAug 14, 2014NC, OH, TX• Biomedix, Inc.

Small Electric Drive (Anspach) – Operational Malfunction (2014)

The affected Small Electric Drive (SED) may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start.

Class IIModerate

FDAAug 14, 2014Nationwide• The Anspach Effort, Inc.

SAM Junctional Tourniquet (Sam Medical) – Snap Hook Failure (2014)

SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112, is recalled because the snap hook on auxiliary strap broke during training demonstration.

Class IIModerate

FDAAug 14, 2014Nationwide• Sam Medical Products

Dimension Vista HbA1c (Siemens) – Sample Recovery Decrease (2014)

In March, Siemens Healthcare Diagnostics issued an Urgent Medical Device Correction for decreased recovery of patient samples with the Dimension Vista® CSA & CSAE Flex® reagent cartridges when whole blood samples are run from Small Sample Containers (SSC). Siemens has confirmed that when whole blood samples are run from SSC, HbA1c values may exhibit a percent bias ranging from - 8.2% t

Class IIModerate

FDAAug 14, 2014Nationwide• Siemens Healthcare Diagnostics, Inc.

Precision Flow Circuit (Vapotherm) – Water Lumen Leak (2014)

Disposable Patient Circuit that allows water to leak into the center gas lumen

Class IIModerate

FDAAug 13, 2014Nationwide• Vapotherm, Inc.

Precision Flow Circuit (Vapotherm) – Water Lumen Leak (2014)

Disposable Patient Circuit that allows water to leak into the center gas lumen

Class IIModerate

FDAAug 13, 2014Nationwide• Vapotherm, Inc.

Precision Flow Circuit (Vapotherm) – Water Lumen Leak (2014)

Disposable Patient Circuit that allows water to leak into the center gas lumen

Class IIModerate

FDAAug 13, 2014Nationwide• Vapotherm, Inc.

Precision Flow Circuit (Vapotherm) – Water Lumen Leak (2014)

Water may leak into the center gas lumen of the Patient Circuit

Class IIModerate

FDAAug 13, 2014Nationwide• Vapotherm, Inc.

Precision Flow Circuit (Vapotherm) – Water Lumen Leak (2014)

Disposable Patient Circuit that allows water to leak into the center gas lumen

Class IIModerate

FDAAug 13, 2014Nationwide• Vapotherm, Inc.

Precision Flow Circuit (Vapotherm) – Water Lumen Leak (2014)

Disposable Patient Circuit that allows water to leak into the center gas lumen

Class IIModerate

FDAAug 13, 2014Nationwide• Vapotherm, Inc.

RENASYS EZ Wound System (Smith & Nephew) – Unapproved Modification (2014)

Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or PreMarket Approval notification.

Class IIModerate

FDAAug 13, 2014Nationwide• Smith & Nephew, Inc.

Propranolol Hydrochloride Injection (Fresenius Kabi) – API Supply Issue (2014)

CGMP Deviations: Citations given to API supplier by the Italian Health Agency AIFA for several critical deficiencies which caused a recall of the API lot used to manufacture Propanolo HCl Injection.

Class IIModerate

FDAAug 13, 2014Nationwide• Fresenius Kabi USA, LLC

1...1158 115911601161 1162...1455

Page 1160 of 1455Next