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 22941–22960 of 29086 results

Sort:

Newest first Oldest first

Little Cremes (Plum) – Choking Hazard (2014)

Increased number of complaints that product is not softening as intended and causes a potential choking hazard in babies and young children,.

Class IIModerate

FDASep 5, 2014Nationwide• Plum, Inc.

Little Cremes (Plum) – Choking Hazard (2014)

Increased number of complaints that product is not softening as intended and causes a potential choking hazard in babies and young children,.

Class IIModerate

Sep 5, 2014

Nationwide

• Plum, Inc.

Jalapeno Bagels (Publix) – Glass Contamination (2014)

May contain pieces of glass and small stones.

Class IIModerate

FDASep 5, 2014AL, FL, GA +1 more• Publix Super Markets, Inc.

ROSA Surgical Device (Zimmer Biomet) – Software Correction (2014)

The software issue described was corrected in the modification to the MXTTOUT controller parameter settings.

Class IIModerate

FDASep 5, 2014Nationwide• Zimmer Biomet, Inc.

Jalapeno Bagels (Wholesome Harvest) – Contamination (2014)

Wholesome Harvest Baking, Inc. ("WHB"), formerly Maple Leaf Bakery, Inc., of Chicago is initiating a voluntary recall of frozen in-store bakery Jalapeno Bagel based on reports of foreign material (glass pieces and stones) in product.

Class IIModerate

FDASep 5, 2014Nationwide• Wholesome Harvest Baking, Inc.

Vantage Panoramic X-Ray (Midmark) – Device Movement Risk (2014)

Failure of the primary collimator may result in unintentional movement of the device. The unintentional movement will not result in the generation of an error message.

Class IIModerate

FDASep 4, 2014AL, AZ, AR +31 more• Midmark Corp dba Progeny Inc

Innova IGS 540 (GE Healthcare) – Imaging Loss Risk (2014)

Loss of imaging - affected devices may experience a loss of real-time interventional imaging and/or gantry motion due to the Electromagnetic (EM) sensitivity of the grid detection mechanism.

Class IIModerate

FDASep 4, 2014CA, CO, FL +2 more• GE Healthcare, LLC

Yellow Rice (Iberia) – Taste Irregularity (2014)

Unpleasant taste and smell. Change of ingredients from Thiamine (Vit B1) to Riboflavin (Vit B2) in one lot.

Class IIModerate

FDASep 4, 2014FL• Iberia Foods Corp.

Rusch Bladder Catheter (Teleflex) – Labeling Omission (2014)

Misbranding: Although the product labeling identifies the catheters as "soft rubber," the Natural Rubber Latex caution statement was not printed on the product label.

Class IIModerate

FDASep 4, 2014Nationwide• Teleflex Medical

Innova 4100IQ (GE Healthcare) – Imaging Loss Risk (2014)

Loss of imaging - affected devices may experience a loss of real-time interventional imaging and/or gantry motion due to the Electromagnetic (EM) sensitivity of the grid detection mechanism.

Class IIModerate

FDASep 4, 2014CA, CO, FL +2 more• GE Healthcare, LLC

Discovery IGS 740 (GE Healthcare) – Imaging Loss Risk (2014)

Loss of imaging - affected devices may experience a loss of real-time interventional imaging and/or gantry motion due to the Electromagnetic (EM) sensitivity of the grid detection mechanism.

Class IIModerate

FDASep 4, 2014CA, CO, FL +2 more• GE Healthcare, LLC

Bupivacaine HCl Injection (Hospira) – Particulate Contamination (2014)

Presence of Particulate Matter: A confirmed customer complaint reported the presence of a brown, rust-colored particle embedded at the bottom of the glass vial.

Class IIModerate

FDASep 4, 2014Nationwide• Hospira Inc.

Aquapak Nebulizer (Teleflex) – Packaging Seal Risk (2014)

Possibility that the nebulizer adaptor packaging may have open or weak seals which may affect the sterility of the adaptor.

Class IIModerate

FDASep 3, 2014Nationwide• Teleflex Medical

Aquapak Adaptor (Teleflex) – Packaging Seal Risk (2014)

Possibility that the nebulizer adaptor packaging may have open or weak seals which may affect the sterility of the adaptor.

Class IIModerate

FDASep 3, 2014Nationwide• Teleflex Medical

RECLAIM Distal Reamer (DePuy) – Screw Fragment Risk (2014)

Specific lots are being recalled due to the potential for the tabs to break, leaving fragments in the patient.

Class IIModerate

FDASep 3, 2014AZ, CA, CO +24 more• DePuy Orthopaedics, Inc.

SPECTRUM Pump (Baxter) – Service Maintenance Issue (2014)

One Service Technician may not have correctly serviced specific Sigma Spectrum Infusion Pumps according to established procedures during the time period of 5/5/2014 through 6/3/2014.

Class IIModerate

FDASep 3, 2014Nationwide• Baxter Healthcare Corp.

AXIOM Luminos (Siemens) – Patient Risk Malfunction (2014)

Two malfunctions posing potential risk to patients were identified with Siemens Ysio Max, AXIOM Luminos dRF Max, Uroskop Omnia Max, and Luminos Agile Max systems with a specific set of serial numbers that will cause lost images due to an automatic Radiology Information System (RIS) worklist update, thus causing examinations to be repeated. Image label may also be displayed incorrectly after images

Class IIModerate

FDASep 2, 2014Nationwide• Siemens Medical Solutions USA, Inc

TI Vectra Plates (Synthes) – Plate Defect (2014)

DePuy Synthes is initiating a voluntary medical device recall of certain lots of the TI Vectra Plates, which is a part of the DePuy Synthes Vectra Anterior Cervical Plate Family of Systems. The Vectra Systems are intended for anterior screw fixation to the cervical spine (C2-C7). It was discovered in certain lots, that the clips are potentially missing from the TI Vectra Plates resulting in the i

Class IIModerate

FDASep 2, 2014AL, CA, CO +10 more• Synthes, Inc.

Aeroneb Professional Nebulizer (Aerogen) – Power Adapter Risk (2014)

Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had broken and dislodged from the body of the adapter prior to use.

Class IIModerate

FDASep 2, 2014Nationwide• Aerogen Ltd.

Aeroneb Professional Nebulizer (Aerogen) – Power Adapter Risk (2014)

Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had broken and dislodged from the body of the adapter prior to use.

Class IIModerate

FDASep 2, 2014Nationwide• Aerogen Ltd.

1...1146 114711481149 1150...1455

Page 1148 of 1455Next