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 201–220 of 297 results

Sort:

Newest first Oldest first

NAImco Inc dba Richmar Inc: Foam Electrodes with Carbon construction: P/N 201-1261, ...

Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was removed.

Class IIModerate

FDANov 30, 2009GA, IN, TN• NAImco Inc dba Richmar Inc

NAImco Inc dba Richmar Inc: Cloth electrodes with Carbon construction: P/N 201-1231...

Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was removed.

Class IIModerate

FDANov 30, 2009GA, IN, TN• NAImco Inc dba Richmar Inc

NAImco Inc dba Richmar Inc: Foam Electrodes with Carbon construction: P/N 201-1261, C...

Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was removed.

Moderate

FDANov 30, 2009GA, IN, TN• NAImco Inc dba Richmar Inc

Millipore Corporation: Millipore Millex Syringe Filter Unit, 33 mm Durapore PVDF...

Membrane integrity defects may allow the passage of viable or non-viable contaminants to pass through the filter.

FDANov 25, 2009Nationwide• Millipore Corporation

Sorin Group USA, Inc.: Sorin / Clearglide EVH Low Profile, REF KTV16, Sterile R,...

Vessel clamping device may break during use.

FDANov 25, 2009Nationwide• Sorin Group USA, Inc.

Sorin Group USA, Inc.: Sorin / Clearglide EVH Small with Scissor, REF KTV17, Ste...

Vessel clamping device may break during use.

FDANov 25, 2009Nationwide• Sorin Group USA, Inc.

Arrow International Inc: Two-Lumen Central Venous Catheterization Kit with Blue Fl...

Q-Syte Component contained in kits was recalled by manufacturer due to the potential for embolism if used with a central venous catheter.

FDANov 24, 2009GA, IN, MD +1 more• Arrow International Inc

CareFusion Corporation: Pyxis Anesthesia System Model 2000 (PAS 2000) Produc...

The recall was initiated because Carefusion has confirmed that when the PAS 2000 drawers due to inaccessability of drawers caused by system down time or lock-up.

Class IIModerate

FDANov 20, 2009Nationwide• CareFusion Corporation

Vascular Solutions, Inc.: Vascular Solutions Pronto-Short Extraction Catheter. Mode...

It was found that three Pronto Short (model 5030) device lots were manufactured and labeled with an expiration date which is inconsistent than the expiration of the included guidewire component. The guidewire is sterilized separately and was realized to have an expiration date of October 31, 2009.

FDANov 20, 2009Nationwide• Vascular Solutions, Inc.

Sunquest Information Systems, Inc.: Sunquest Application Interfacing Outbound Phlebotomy Poin...

The recall was initiated because Sunquest Information System has confirmed reports of an Outbound Phlebotomy Point of Care (POC) interface is combining patient orders inappropriately.

Class IIModerate

FDANov 19, 2009Nationwide• Sunquest Information Systems, Inc.

Biosense Webster, Inc.: CARTO 3 V1.05(FG-5400-00). The CARTO 3 V1.05 System is...

The recall was initiated because Biosense Webster has become aware of information regarding a potential hazard that may occur during the operation of a Bloom EP Stimulator device in conjunction with RF generators and other electrophysiology (EP) equipment, including the CARTO 3 Electropysiology Mapping System.

Class IIModerate

FDANov 17, 2009Nationwide• Biosense Webster, Inc.

Abaxis Inc: Piccolo Comprehensive Metabolic Panel Reagent Disc, 10-pa...

Wrong barcode applied to a lot of items, which may result in incorrect calibration factors and results.

FDANov 16, 2009Nationwide• Abaxis Inc

Becton Dickinson & Co.: BD BACTEC(TM) Lytic 10 Anaerobic/F Medium, catalog 442265...

The draw volume on test tubes of blood culture medium is marked with graduations that may be confusing for healthcare practitioners using the tubes for appropriate collection of patient samples for microbiological laboratory testing.

FDANov 11, 2009Nationwide• Becton Dickinson & Co.

Becton Dickinson & Co.: BD BACTEC(TM) Plus + Aerobic/F Medium, catalog 442192, pa...

The draw volume on test tubes of blood culture medium is marked with graduations that may be confusing for healthcare practitioners using the tubes for appropriate collection of patient samples for microbiological laboratory testing.

FDANov 11, 2009Nationwide• Becton Dickinson & Co.

Becton Dickinson & Co.: BD BACTEC(TM) Standard 10 Aerobic/F Medium, catalog 44226...

The draw volume on test tubes of blood culture medium is marked with graduations that may be confusing for healthcare practitioners using the tubes for appropriate collection of patient samples for microbiological laboratory testing.

FDANov 11, 2009Nationwide• Becton Dickinson & Co.

Pointe Scientific, Inc.: Calcium (CPC) R1 Reagent Set. Pointe Scientific Liquid C...

Non-compliance with the Good Manufacturing Practice regulations, as the manufacturing process for this product had not been validated.

FDANov 10, 2009Nationwide• Pointe Scientific, Inc.

Pointe Scientific, Inc.: Calcium Reagent Set. Pointe Scientific Liquid Hitachi Ca...

Non-compliance with the Good Manufacturing Practice regulations, as the manufacturing process for this product had not been validated.

FDANov 10, 2009Nationwide• Pointe Scientific, Inc.

GE OEC Medical Systems, Inc: 892.1650 Image-intensified fluoroscopic x-ray system; the...

GE OEC is recalling certain 9800 Image Intensified Flouroscopic x-ray systems due to customer complaint analysis showing that a replacement Hitachi 160 GB Hard Drive, when installed on certain models is susceptible of causing unanticipated system shut downs, no boots, data loss or data mix, or unexpected hard drive corruption.

Class IIModerate

FDANov 6, 2009Nationwide• GE OEC Medical Systems, Inc

Philips Medical Systems: Philips Heartstart (HS1) Onsite Automated External Defibr...

Potential for failure of a capacitor during use which would prevent the AED from delivering effective defibrillation therapy when indicated.

FDANov 2, 2009Nationwide• Philips Medical Systems

Spire Biomedical, Inc. One Patriots Park: 28CM DECATHLON FUNNEL TIP CATHETER Model: DF23SH28-100 D...

There is a possibility that the catheter tubing could separate from the hub/bifurcation of the device. If this occurs, bleeding is the primary clinical complication likely to result from catheter tubing/hub separation. A second potential clinical complication is air embolism, particularly for the segment of the patient population that develops negative central venous pressure during normal respira

FDAOct 23, 2009Nationwide• Spire Biomedical, Inc. One Patriots Park

1...9 101112 13...15

Page 11 of 15Next