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. Not affiliated with any government agency. Always verify information with official sources.

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 ↗

Not a government website.

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 1–20 of 1008 results

Sort:

Newest first Oldest first

Pacemaker Implant Pack (Medline) – Subpotent Iodine Prep (2017)

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

FDASep 21, 2017Nationwide• Medline Industries Inc

Catheter Insertion Kit (Medline) – Subpotent Iodine Prep (2017)

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

FDASep 21, 2017Nationwide• Medline Industries Inc

Catheter Care Lidded Tray (Medline) – Subpotent Iodine Prep (2017)

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

Class II

FDASep 21, 2017Nationwide• Medline Industries Inc

Hip Replacement Kit (Medline) – Subpotent Iodine Prep (2017)

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

FDASep 21, 2017Nationwide• Medline Industries Inc

Catheter Insertion Tray (Medline) – Subpotent Iodine Prep (2017)

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

FDASep 21, 2017Nationwide• Medline Industries Inc

Siemens Healthcare Diagnostics Inc: RAPIDLab 1245 System; Siemens Material Number: 10321844,...

Neonatal bilirubin (nBili) parameter may have increased variability when the nBili concentration is greater than 12 mg/dl and the tHb concentration exceeds the upper reportable range of greater than 25 g/dl.

FDADec 30, 2014Nationwide• Siemens Healthcare Diagnostics Inc

Siemens Healthcare Diagnostics Inc: RAPIDPoint 500 Blood Gas Analyzer; Siemens Material Numbe...

Neonatal bilirubin (nBili) parameter may have increased variability when the nBili concentration is greater than 12 mg/dl and the tHb concentration exceeds the upper reportable range of greater than 25 g/dl.

FDADec 30, 2014Nationwide• Siemens Healthcare Diagnostics Inc

Siemens Healthcare Diagnostics Inc: RAPIDPoint 405 Blood Gas Analyzer; Siemens Material Numbe...

Neonatal bilirubin (nBili) parameter may have increased variability when the nBili concentration is greater than 12 mg/dl and the tHb concentration exceeds the upper reportable range of greater than 25 g/dl.

FDADec 30, 2014Nationwide• Siemens Healthcare Diagnostics Inc

Siemens Healthcare Diagnostics Inc: RAPIDLab 1265 System; Siemens Material Number: 10491395,...

Neonatal bilirubin (nBili) parameter may have increased variability when the nBili concentration is greater than 12 mg/dl and the tHb concentration exceeds the upper reportable range of greater than 25 g/dl.

FDADec 30, 2014Nationwide• Siemens Healthcare Diagnostics Inc

Baxter Corporation Englewood: Baxter, Self-Righting Syringe Tip Caps, Self-Righting DIS...

Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.

FDADec 29, 2014Nationwide• Baxter Corporation Englewood

Dick's Sporting Goods: Fitness Gear Inversion table (Style STE00059FG or Style S...

Reports of customers falling from the Inversion Table and sustaining injuries. The Inversion Table is a fitness product, not a medical device. DSG removed medical claims from product labels and advertising.

FDADec 29, 2014Nationwide• Dick's Sporting Goods

Shape Medical Systems, Inc: Shape-HF Cardiopulmonary Testing System Disposable Patien...

This recall has been initiated because use of the impacted DPIs could result in erroneous testing results potentially leading to incorrect diagnosis and incorrect treatment. The magnitude of error for VO2 or VCO2 parameters could be approximately 20% with use of the impacted product.

FDADec 23, 2014AZ, FL, GA +8 more• Shape Medical Systems, Inc

Philips Medical Systems, Inc.: HeartStart MRx monitor/defibrillator Models M3535A, M353...

MRx monitor/defibrillator could reboot at an indeterminate time, potentially causing therapy to be interrupted or delayed

FDADec 23, 2014Nationwide• Philips Medical Systems, Inc.

Fresenius Kabi USA, LLC: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION, USP) 100 USP un...

The lot failed pH specification.

FDADec 19, 2014Nationwide• Fresenius Kabi USA, LLC

Elekta, Inc.: Monaco radiation therapy treatment planning system. ...

Incorrect CT to ED when using the Monaco Image Statistics Tool.

FDADec 19, 2014Nationwide• Elekta, Inc.

GE Healthcare: GE Healthcare Automatic Mobile X-Ray (AMX) Series: Brivo...

An issue was identified with the mAs accuracy check performed on the system that could result in inaccuracies in the 10% to 20% range for exposure times longer than 15 msec.

FDADec 19, 2014AZ, FL, GA +2 more• GE Healthcare

GE Healthcare: GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optim...

An issue was identified with the mAs accuracy check performed on the system that could result in inaccuracies in the 10% to 20% range for exposure times longer than 15 msec.

FDADec 19, 2014AZ, FL, GA +2 more• GE Healthcare

Elekta, Inc.: Focal Sim radiation therapy treatment planning system

Incorrect CT to ED when using the Monaco Image Statistics Tool.

FDADec 19, 2014Nationwide• Elekta, Inc.

Integra LifeSciences Corporation: The MAYFIELD¿ Ultra 360 Base Unit for head positioner, on...

Through an investigation of complaints, Integra found that there is the possibility for the locking handle mechanism of the Base Units to fail during use.

FDADec 19, 2014Nationwide• Integra LifeSciences Corporation

Sunrise Medical (US) LLC: Quickie Q7 Adult Rigid Wheelchair Model EIR4.

There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.

FDADec 19, 2014Nationwide• Sunrise Medical (US) LLC

Previous

12 3...51

Page 1 of 51Next