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 5001–5020 of 11714 results

Sort:

Newest first Oldest first

COBALT DR MRI SureScan Defibrillator (Medtronic) – manufacturing defect (2024)

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

FDAApr 16, 2024Nationwide• Medtronic Inc.

Cobalt XT HF CDT-D Defibrillator (Medtronic) – manufacturing defect (2024)

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

FDAApr 16, 2024Nationwide• Medtronic Inc.

COBALT VR MRI SureScan Defibrillator (Medtronic) – manufacturing defect (2024)

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

High

FDAApr 16, 2024Nationwide• Medtronic Inc.

COBALT XT HF CRT-D Defibrillator (Medtronic) – manufacturing defect (2024)

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

FDAApr 16, 2024Nationwide• Medtronic Inc.

Cobalt XT DR MRI SureScan Defibrillator (Medtronic) – manufacturing defect (2024)

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

FDAApr 16, 2024Nationwide• Medtronic Inc.

Stryker Blueprint Software (Tornier) – case planning bug (2024)

The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations that are incompatible and do not have regulatory approval.

FDAApr 16, 2024Nationwide• Tornier S.A.S. 161 Rue Lavoisier Montbonnot St Martin France

CARDIOHELP-i System (Maquet) – patient leakage current (2024)

The firm identified that the measured patient leakage current in some devices significantly exceeded expected levels.

FDAApr 15, 2024Nationwide• Maquet Medical Systems USA

BD Pyxis MedStation Auxiliary Tower (CareFusion) – fluid ingress risk (2024)

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

FDAApr 15, 2024Nationwide• CareFusion 303, Inc.

Tri-Staple 2.0 Reload (Unknown) – cartridge damage risk (2024)

Potential damage to the cartridge can result in poor staple formation and/or incomplete staple line, may cause a delay in surgery

FDAApr 15, 2024Nationwide

BD Pyxis Anesthesia Station (CareFusion) – fluid ingress risk (2024)

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

FDAApr 15, 2024Nationwide• CareFusion 303, Inc.

Incisive CT X-Ray System (Philips) – mounting box compromise (2024)

Metal mounting box on the rotating scanner on rotor (heat change box) located within the Incisive CT system, may become compromised, resulting in potential contact with other gantry components located within the Incisive CT system during rotation. Resulting in a fragment of a damaged component expelled at a low velocity

FDAApr 15, 2024Nationwide• Philips North America Llc

BD Pyxis MedStation Auxiliary Tower (CareFusion) – fluid ingress risk (2024)

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

FDAApr 15, 2024Nationwide• CareFusion 303, Inc.

BD Pyxis MedStation 4000 System (CareFusion) – fluid ingress risk (2024)

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

FDAApr 15, 2024Nationwide• CareFusion 303, Inc.

Total Knee Arthroplasty System (Stryker) – software error (2024)

Application software intended to be deployed on Mako 3.0, part number 209999, and Mako 3.1, part number 219999, observed an increase in the Software Error #3 (SE3) error code when a Mako System shutdown or a Mako System restart is not performed prior to switching between applications (i.e. TKA to THA), resulting in delay in treatment

FDAApr 15, 2024Nationwide• Stryker Orthopaedics

BD Pyxis Anesthesia Station 4000 (CareFusion) – fluid ingress risk (2024)

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

FDAApr 15, 2024Nationwide• CareFusion 303, Inc.

BD Pyxis MedStation (CareFusion) – fluid ingress risk (2024)

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

FDAApr 15, 2024Nationwide• CareFusion 303, Inc.

Organic Black Chia Seeds (Walmart) – Salmonella Risk (2024)

Salmonella contamination

FDAApr 15, 2024AL, CA, CO +9 more• NATURAL SOURCING INTERNATIONAL,LLC

MyoSPECT System (GE Medical) – lead cover handle risk (2024)

There is a potential issue regarding the service handles for the internal lead (Pb) covers in that the handles could loosen or release which could cause a cover to drop potentially resulting in injury to service personnel due to the weight of the cover.

FDAApr 15, 2024Nationwide• GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING 4, Hayozma St Tirat Carmel Israel

APTUS TriLock Screw (Medartis) – incorrect length (2024)

Screw is 16mm long instead of 22mm long.

FDAApr 12, 2024Nationwide• Medartis Inc.

Arial Mobile Application (Securitas) – alert restart issue (2024)

The Arial Mobile Application utilizing Apple iOS 17.4 and iOS 17.5 is frequently restarting causing the app to receive alerts for all pending alarm notifications and other events when the app restarts, experience difficulty in placing and maintaining staff-to-staff phone calls, and frequently appears offline while the app restarts.

FDAApr 11, 2024Nationwide• Securitas Healthcare LLC

1...249 250251252 253...586

Page 251 of 586Next