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 6941–6960 of 11714 results

Sort:

Newest first Oldest first

OES Bronchofiberscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

FRED Flow Re-Direction Endoluminal Device (MICROVENTION) – Incorrect Inner Stent Length (2023)

Intracranial aneurysm flow diverter device may be manufactured with an incorrect inner stent length and may not perform as intended.

FDAJun 7, 2023Nationwide• MICROVENTION INC.

BeamAdjust Software (PTW-FREIBURG) – Calibration File Error (2023)

Generated calibration file will not be correct in case of a relative calibration of an OCTAVIUS Detector 1000 or OCTAVIUS Detector 1600, if a Tiff file or a DICOM data set is used as reference matrix. Therefore, the measurement result will be incorrect by using such a calibration file.

Low

FDAJun 7, 2023Nationwide• PTW-FREIBURG Lorracher Str. 7 Freiburg Im Breisgau Germany

Vanta AdaptiveStim Neurostimulator (Medtronic) – Cardioversion Damage (2023)

A cardioversion procedure may damage the electronics in the Vanta INS device, making the INS unresponsive and non-functional. As of April 19, 2023, Medtronic has received a total of two complaints concerning this issue from patients implanted with a Vanta INS, both of which have resulted in explant procedures.

FDAJun 6, 2023Nationwide• Medtronic Neuromodulation

OmniTom X-ray CT System (NeuroLogica) – Device Mobility Risks (2023)

1. Wheels loosening over time with use of the device could lead to the inability to effectively drive the device and could lead to delay in patient treatment. 2.Batteries used to power the NL5000 device contain contaminated boards, which may impact the ability to power on the device, this could lead to delay for patient treatment

FDAJun 6, 2023Nationwide• NeuroLogica Corporation

Vios Bedside Monitor (Murata Vios) – Pulse Oximeter Sensor Failure (2023)

A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system.

FDAJun 6, 2023Nationwide• Murata Vios, Inc.

NanoZoomer S360MD Slide Scanner (Hamamatsu) – Incorrect Barcode Identification (2023)

If the wrong barcode information is recorded in the NDPi file, a pathologist may refer to the whole slide image (WSI) of a different patient.

FDAJun 6, 2023NY• Hamamatsu Corporation

Catalyft LS Interbody System (Medtronic) – Geometry Specification Issue (2023)

There is the potential for out of specification device geometries. widths, lengths, heights, and lordotic angles to accommodate patient anatomy. These devices can be inserted between two lumbar or lumbosacral vertebral bodies to give support and correction during lumbar interbody fusion surgeries. Implants have a central cavity that allows them to be packed with autogenous bone graft and/or allograft bone graft comprised of cancellous and/or Corticocancellous bone, and/or demineralized allograft bone with bone marrow aspirate.

FDAJun 6, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Cios Select X-ray System (Siemens) – Plexiglass Cover Issue (2023)

Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric shock exists (e.g., ingress of a large amount of liquid following the plexiglass dropping off, at the same time the user or operator happens to touch the liquid on the cover which is connected to the internal live parts).

FDAJun 5, 2023Nationwide• Siemens Medical Solutions USA, Inc

Verigene Enteric Pathogens Test (Luminex) – Test Kit Reliability (2023)

It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit (Part No. 20-005-022) and the VERIGENE Enteric Pathogens Nucleic Acid Test Kit (Part No. 20-005-023) could provide a false-negative result due to hydrophobic characteristics in specific FLOQSwab lots.

FDAJun 5, 2023Nationwide• Luminex Corporation

VITROS Troponin I ES Reagent (ORTHO-CLINICAL) – Incorrect Wells (2023)

Reagent packs could potentially contain incorrect wells, which will generate incorrect, and potentially false negative, results.

FDAJun 5, 2023Nationwide• ORTHO-CLINICAL DIAGNOSTICS Felindre Meadows Bridgend United Kingdom

Cardiosave Hybrid IABP (Datascope) – Battery Charging Failure (2023)

IABP may lose the ability to charge batteries in one or both bay slots. Therapy may be interrupted if batteries fail to charge and the device is disconnected from AC power. Low battery alarms may alert the User to the issue prior to interruption of therapy.

FDAJun 5, 2023Nationwide• Datascope Corp.

Cardiosave Rescue IABP (Datascope) – Battery Charging Failure (2023)

IABP may lose the ability to charge batteries in one or both bay slots. Therapy may be interrupted if batteries fail to charge and the device is disconnected from AC power. Low battery alarms may alert the User to the issue prior to interruption of therapy.

FDAJun 5, 2023Nationwide• Datascope Corp.

Shoulder GPS Impactor Handle (Exactech) – Mechanism Dislodgement (2023)

The ball and spring housed within the locking mechanism of the handle can dislodge during disassembly or during impaction.

FDAJun 5, 2023AR, CA, CO +23 more• Exactech, Inc.

Perifix Epidural Kit (B. Braun) – Incorrect Filter Straw (2023)

Kits were assembled with the incorrect Filter Straw.

FDAJun 5, 2023Nationwide• B. Braun Medical, Inc.

Cardiosave Rescue IABP (Datascope) – Power Board Failure (2023)

An unexpected shutdown of the IABP may occur due to failures of tantalum capacitors in the Power Management Board and/or Solenoid Board. This issue may lead to an unexpected interruption of therapy.

FDAJun 5, 2023Nationwide• Datascope Corp.

VERIGENE C. Difficile Test (Luminex) – Test Kit Reliability (2023)

It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit (Part No. 20-005-022) and the VERIGENE Enteric Pathogens Nucleic Acid Test Kit (Part No. 20-005-023) could provide a false-negative result due to hydrophobic characteristics in specific FLOQSwab lots.

FDAJun 5, 2023Nationwide• Luminex Corporation

Ergo Impactor Handle (Exactech) – Mechanism Dislodgement (2023)

The ball and spring housed within the locking mechanism of the handle can dislodge during disassembly or during impaction.

FDAJun 5, 2023AR, CA, CO +23 more• Exactech, Inc.

Design Options Epidural Kit (B. Braun) – Incorrect Filter Straw (2023)

Kits were assembled with the incorrect Filter Straw.

FDAJun 5, 2023Nationwide• B. Braun Medical, Inc.

Cardiosave Hybrid IABP (Datascope) – Power Board Failure (2023)

An unexpected shutdown of the IABP may occur due to failures of tantalum capacitors in the Power Management Board and/or Solenoid Board. This issue may lead to an unexpected interruption of therapy.

FDAJun 5, 2023Nationwide• Datascope Corp.

1...346 347348349 350...586

Page 348 of 586Next