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 6881–6900 of 8389 results

Sort:

Newest first Oldest first

Plus 30 Priority Pack (Abbott Vascular) – Connection Leak Risk (2022)

Due to an increase in complaint trend for leaks and intermittent/loose connections.

FDAMar 11, 2022Nationwide• Abbott Vascular

Abbott Priority Pack (Abbott Vascular) – Connection Leak Risk (2022)

Due to an increase in complaint trend for leaks and intermittent/loose connections.

FDAMar 11, 2022Nationwide• Abbott Vascular

Abbott Priority Pack (Abbott Vascular) – Connection Leak Risk (2022)

Due to an increase in complaint trend for leaks and intermittent/loose connections.

FDAMar 11, 2022Nationwide• Abbott Vascular

Virus Counter Platform (Sartorius) – Non-Medical Device (2022)

The Virus Counter is an automated laboratory instrument that enables rapid quantification of intact viruses in solution. This instrument is not a medical device. The virus quantification is used in process development and manufacturing of various biotechnology products such as vaccines, gene therapy and personalized immunotherapy. Device is a Class 1 laser flow cytometer.

FDAMar 11, 2022Nationwide• Sartorius Corporation

INDEFLATOR Plus 30 (Abbott Vascular) – Connection Leak Risk (2022)

Due to an increase in complaint trend for leaks and intermittent/loose connections.

FDAMar 11, 2022Nationwide• Abbott Vascular

20/30 INDEFLATOR (Abbott Vascular) – Connection Leak Risk (2022)

Due to an increase in complaint trend for leaks and intermittent/loose connections.

FDAMar 11, 2022Nationwide• Abbott Vascular

Gallant HF Defibrillator (St. Jude Medical) – Bluetooth Malfunction (2022)

Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

Merlin 2 PCS Programmer (St. Jude Medical) – Software Anomaly (2022)

Laceration Risk

Due to a programmer software anomaly under very specific circumstance when executing a pacing capture Decrement Test in-clinic on implantable cardioverter and cardiac resynchronization therapy defibrillator devices, the programmer may continue to execute the Decrement Test instead of terminating the test and restoring the permanent programmed pacing parameters.

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

Merlin PCS Programmer (St. Jude Medical) – Software Anomaly (2022)

Laceration Risk

Due to a programmer software anomaly under very specific circumstance when executing a pacing capture Decrement Test in-clinic on implantable cardioverter and cardiac resynchronization therapy defibrillator devices, the programmer may continue to execute the Decrement Test instead of terminating the test and restoring the permanent programmed pacing parameters.

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

Gallant DR Defibrillator (St. Jude Medical) – Bluetooth Malfunction (2022)

Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

Gallant VR Defibrillator (St. Jude Medical) – Bluetooth Malfunction (2022)

Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

EasyFuse Dynamic Compression System (Wright Medical) – Instrument Jam Risk (2022)

The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.

FDAMar 10, 2022FL, NC, OH +1 more• Wright Medical Technology, Inc.

Medline Laryngeal Masks (Medline) – Mask Disconnection Risk (2022)

The mask cuff may disconnect from the device's breathing tube.

FDAMar 9, 2022Nationwide• MEDLINE INDUSTRIES, LP Northfield

ROTAWIRE Drive (Boston Scientific) – Sterility Compromise (2022)

Pouch seals may be open, compromising sterility.

FDAMar 8, 2022IN• Boston Scientific Corporation

EVIS EXERA Bronchofibervideoscope (Olympus) – Reprocessing Instructions (2022)

Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization

FDAMar 8, 2022Nationwide• Olympus Corporation of the Americas

EVIS EXERA Bronchovideoscope (Olympus) – Reprocessing Instructions (2022)

Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization

FDAMar 8, 2022Nationwide• Olympus Corporation of the Americas

ARCHITECT Myoglobin Calibrators (Abbott) – Testing Accuracy Issue (2022)

This calibrator lot did not meet acceptance criteria during ongoing stability testing. When a calibration is performed with this lot, controls may exceed the specified range in the Instructions for Use (IFU).

FDAMar 8, 2022Nationwide• Abbott Laboratories

EVIS EXERA II Bronchovideoscope (Olympus) – Reprocessing Instructions (2022)

Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization

FDAMar 8, 2022Nationwide• Olympus Corporation of the Americas

OnGuard2 CSTD Bag Adaptor (Simplivia) – Medication Spillage Risk (2022)

Disconnection of the OnGuard2 Bag Adaptor SP from infusion bags which may result in spillage of hazardous medications.

FDAMar 8, 2022Nationwide• SIMPLIVIA HEALTHCARE LTD. NORTH IND. ZONE, (MIGADA PLANT) NORTH IND. ZONE PoBOX

OES Bronchofiberscope (Olympus) – Reprocessing Instructions (2022)

Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization

FDAMar 8, 2022Nationwide• Olympus Corporation of the Americas

1...343 344345346 347...420

Page 345 of 420Next