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 7101–7120 of 11714 results

Sort:

Newest first Oldest first

Medline Probe Cover Kits (Medline) – Barrier Seam Inadequacy (2023)

Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

FDAMay 18, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Aesculap Surgical Needle (Aesculap) – Product Code Mismatch (2023)

Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.

FDAMay 18, 2023Nationwide• Aesculap Implant Systems LLC

QUADROX-i Pediatric (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

Very High

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-i Small (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-i Neonatal (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

Venous Hardshell Cardiotomy Reservoir (Maquet) – Packaging Pinhole Risk (2023)

Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-i Small Adult (Maquet) – Packaging Pinhole Risk (2023)

Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-iD Adult (Maquet) – Packaging Pinhole Risk (2023)

Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-iD Adult (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-i Small Adult (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

Access Hybritech p2PSA Reagent (Beckman) – Blocking Reagent Concentration (2023)

Reagent lot numbers include an insufficient concentration of blocking reagent.

FDAMay 17, 2023CA, CO, CT +16 more• Beckman Coulter, Inc.

HeartWare VAD System (Heartware) – Monitor Logfile Issue (2023)

Medtronic has identified that the logfiles downloaded from the recently updated Model 1521 monitors (Serial Numbers: MON4xxxxxx for OUS and MON5xxxxxx for US), are unable to be processed by the Autologs web portal.

FDAMay 16, 2023Nationwide• Heartware, Inc.

Aptio Automation SRM (Siemens) – Test Result Firmware Error (2023)

A firmware error may lead to an incorrect association of test result(s) to a sample ID and therefore to an incorrect patient result. The mis-association of test results, or a delay in testing, may occur when all the conditions listed below occur within a few milliseconds timeframe of each other: - The SRM module is releasing a sample tube (Tube A) just placed into the carrier - Another sample tube (Tube B) is erroneously not diverted into the SRM module buffer - There is divert gate malfunction and a narrow timing window Only in this specific scenario, Tube A may be released by the module as Tube B due to a miscommunication between the module firmware and the Automation software without a unique error message being generated. The Automation System loses the traceability of Tube A. It manages both Tube A (incorrectly identified as Tube B) and the real Tube B according to the pending test orders (not yet performed) on Tube B.

FDAMay 16, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Aeris Balloon Dilation Catheter (Bryan Medical) – Mislabeling (2023)

Devices were mislabeled.

FDAMay 16, 2023Nationwide• Bryan Medical Inc

Draeger Softbed Resuscitaire (Draeger) – Weight Display Problem (2023)

The Resuscitaire Infant Radiant Warmer with the optional scale could display inaccurate weight values.

FDAMay 16, 2023Nationwide• Draeger Medical Systems, Inc.

Philips Respironics V60 Ventilator (DRE Medical) – Gas Fitting Risk (2023)

Devices were imported with Japanese Language and NIST Oxygen Gas Fittings and retrofitted, may pose a serious health risk as the gas pathway of these devices may be contaminated.

FDAMay 15, 2023CA, FL• DRE Medical Group Inc

Field Upgrade Kits (GE OEC) – Image Intensifier Detachment (2023)

Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, hematoma, contusion, bruise, pain.

FDAMay 15, 2023Nationwide• GE OEC Medical Systems, Inc

Procedural Kits (Medline) – Ultrasound Gel Sterility (2023)

Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

FDAMay 15, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

OEC Flexiview 8800 Systems (GE OEC) – Image Intensifier Detachment (2023)

Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, hematoma, contusion, bruise, pain.

FDAMay 15, 2023Nationwide• GE OEC Medical Systems, Inc

Probe Cover Kits (Medline) – Ultrasound Gel Sterility (2023)

Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

FDAMay 15, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

1...354 355356357 358...586

Page 356 of 586Next