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 4881–4900 of 22534 results

Sort:

Newest first Oldest first

Legion FMS Pak (Alcon Research, LTD.) – plastic contamination (2023)

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

FDAJun 28, 2023Nationwide• Alcon Research, LTD.

Phaco Standalone Tips (Alcon Research, LTD.) – plastic contamination (2023)

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

FDAJun 28, 2023Nationwide• Alcon Research, LTD.

stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to... (Stryker Corporation) – there is potential the device inside ... (2023)

There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).

Moderate

FDAJun 28, 2023Nationwide• Stryker Corporation

ACCESSRAIL Platform (Standard Blade) Part Number SB-1000,... (Maquet Cardiovascular, LLC) – the standard blade may not securely l... (2023)

The Standard Blade may not securely latch onto the Activator Drive. This may result in the inability to stabilize and position or may result in the loss of stabilization and positioning of heart, release of device component into the patient, and/or a procedural delay and/or conversion.

FDAJun 28, 2023Nationwide• Maquet Cardiovascular, LLC

ACROBAT-i Vacuum Stabilizer System, Part Number C-OM-1000... (Maquet Cardiovascular, LLC) – the standard blade may not securely l... (2023)

The Standard Blade may not securely latch onto the Activator Drive. This may result in the inability to stabilize and position or may result in the loss of stabilization and positioning of heart, release of device component into the patient, and/or a procedural delay and/or conversion.

FDAJun 28, 2023Nationwide• Maquet Cardiovascular, LLC

ACROBAT V Vacuum Off-Pump System, Part Number C-OM-9100S.... (Maquet Cardiovascular, LLC) – the standard blade may not securely l... (2023)

The Standard Blade may not securely latch onto the Activator Drive. This may result in the inability to stabilize and position or may result in the loss of stabilization and positioning of heart, release of device component into the patient, and/or a procedural delay and/or conversion.

FDAJun 28, 2023Nationwide• Maquet Cardiovascular, LLC

Alcon Custom Pak (Alcon Research, LTD.) – plastic contamination (2023)

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

FDAJun 28, 2023Nationwide• Alcon Research, LTD.

Centurion FMS Pak (Alcon Research, LTD.) – plastic contamination (2023)

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

FDAJun 28, 2023Nationwide• Alcon Research, LTD.

ACROBAT SUV Vacuum Off-Pump System, Part Number C-OM-9000... (Maquet Cardiovascular, LLC) – the standard blade may not securely l... (2023)

The Standard Blade may not securely latch onto the Activator Drive. This may result in the inability to stabilize and position or may result in the loss of stabilization and positioning of heart, release of device component into the patient, and/or a procedural delay and/or conversion.

FDAJun 28, 2023Nationwide• Maquet Cardiovascular, LLC

Constellation Procedure Pak (Alcon Research, LTD.) – plastic contamination (2023)

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

FDAJun 28, 2023Nationwide• Alcon Research, LTD.

Medtronic REF 46915 Duet External Drainage and Monitoring... (Medtronic Neurosurgery) – product labeling contains incorrect e... (2023)

Product labeling contains incorrect expiration date

FDAJun 28, 2023Nationwide• Medtronic Neurosurgery

The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) ... (Stryker Corporation) – there is potential the device inside ... (2023)

There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-030 but package contains a 5820-107-530 device).

FDAJun 28, 2023Nationwide• Stryker Corporation

stryker 3.0MM Precision Neuro Match Head, REF 5820-107-53... (Stryker Corporation) – there is potential the device inside ... (2023)

There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).

FDAJun 28, 2023Nationwide• Stryker Corporation

Infinity FMS Pak (Alcon Research, LTD.) – plastic contamination (2023)

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

FDAJun 28, 2023Nationwide• Alcon Research, LTD.

Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral ... (Zimmer, Inc.) – thread form issue of the locking hole... (2023)

Thread form issue of the locking holes in that the locking screws would not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock.

FDAJun 27, 2023AZ, AR, ME +7 more• Zimmer, Inc.

ISee Ortho-K Lens (PARAGON VISION SCIENCES, Inc) – manufactured lenses are not covered b... (2023)

Manufactured lenses are not covered by existing FDA approval

FDAJun 26, 2023Nationwide• PARAGON VISION SCIENCES, Inc

Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound ... (Digisonics, Inc) – software issue (2023)

Software issue

FDAJun 26, 2023AK, CA, GA +16 more• Digisonics, Inc

Fargo Ortho-K Lens (PARAGON VISION SCIENCES, Inc) – manufactured lenses are not covered b... (2023)

Manufactured lenses are not covered by existing FDA approval

FDAJun 26, 2023Nationwide• PARAGON VISION SCIENCES, Inc

MEGA 7.5Fr.IAB , Intra-Aortic Balloon Catheter and Access... (Datascope Corp.) – during iab catheter insertion, the in... (2023)

During IAB catheter insertion, the introducer dilator may fracture at the hub, leaving the body of the introducer dilator housed within the sheath. Risks to health include damage to the femoral artery, descending aorta, or embolization; surgical intervention and delay of IAB therapy may also result. Firm has received 10 complaints, including 3 serious adverse events and 1 patient death.

FDAJun 23, 2023Nationwide• Datascope Corp.

LINEAR 7.5Fr IAB Catheter (Datascope) – Dilator Fracture Risk (2023)

During IAB catheter insertion, the introducer dilator may fracture at the hub, leaving the body of the introducer dilator housed within the sheath. Risks to health include damage to the femoral artery, descending aorta, or embolization; surgical intervention and delay of IAB therapy may also result. Firm has received 10 complaints, including 3 serious adverse events and 1 patient death.

FDAJun 23, 2023Nationwide• Datascope Corp.

1...243 244245246 247...1127

Page 245 of 1127Next