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 63961–63980 of 68218 results

Sort:

Newest first Oldest first

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew Suture Passer 12 inch Part Number: 7209166

Product is labeled as reusable but there is a potential that the cannulated handle of the product cannot be cleaned adequately following use.

FDAMar 1, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

GE OEC Medical Systems, Inc: OEC 9900 Elite image-intensified fluoroscopic x-ray syste...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC FluoroTrak 9800 PLUS, image-intensified fluoroscopic ...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 image-intensified fluoroscopic x-ray system, GE ...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 Plus (Fluorotrak), Image-intensified fluoroscopi...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

Mizuho Orthopedic Systems Inc: OSI ProFx Operating Room Table 6850 , Pelvic Reconstructi...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Mizuho Orthopedic Systems Inc: OSI, Allegro 6800 Imaging Table (Operating), single pedes...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Mizuho Orthopedic Systems Inc: OSI, 6822 IntraOp Series Tables, Operating Room tables, O...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Roche Diagnostics Corp.: CoaguChek brand PT Test Strips; U.S. Catalog Number 31162...

The product was erroneously distributed to home users in contrast to its use for healthcare professionals only.

FDAFeb 28, 2007Nationwide• Roche Diagnostics Corp.

Cook, Inc.: Cook ATB Advance PTA Dilatation Catheter, French size 5, ...

Mislabeled as to size: The outer label reads 7-4.0 balloon, when the balloon is actually 5-2.0.

FDAFeb 28, 2007IL, NC, SC• Cook, Inc.

American Diagnostica, Inc.: American Diagnostica Inc. ACTICLOT dPT Reference 824 i...

Stability of product not assured. An increase of clotting time for both normal and abnormal plasmas

FDAFeb 28, 2007Nationwide• American Diagnostica, Inc.

Philips Medical Systems: Philips HeartStart FR2+ Defibrillator Automated External...

Failure of tactile switches on one of two printed circuit board assemblies (PCBA) used in the FR2+ device. Potential delay or prevention of shock treatment due to PCBA board contamination, causing intermittent switch operation.

FDAFeb 28, 2007Nationwide• Philips Medical Systems

Siemens Medical Solutions USA, Inc: Si emans Simiae NT Cassette Holder Electronic Imaging Dev...

Loose Mounting Screws -- Cassette holder may become loose and result in the device dislodging and colliding with the patient.

FDAFeb 27, 2007AL, AZ, AR +28 more• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Si emans Evansi, with patient table, Part No: 44 81 586, ...

Loose Mounting Screws -- Cassette holder may become loose and result in the device dislodging and colliding with the patient.

FDAFeb 27, 2007AL, AZ, AR +28 more• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Si emans Simiae 3000 Cassette Holder Electronic Imaging d...

Loose Mounting Screws -- Cassette holder may become loose and result in the device dislodging and colliding with the patient.

FDAFeb 27, 2007AL, AZ, AR +28 more• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Si emans Simview NT Cassette Holder Electronic Imaging De...

Loose Mounting Screws -- Cassette holder may become loose and result in the device dislodging and colliding with the patient.

FDAFeb 27, 2007AL, AZ, AR +28 more• Siemens Medical Solutions USA, Inc

Bio-Logic Systems Corp: Bio-logic-Ceegraph/Sleepscan Netlink Traveler, Bio-logic ...

Battery and Battery Compartment; incorrect placement in the Netlink Traveler unit which caused a short in the wiring of the battery pack and overheating.

FDAFeb 26, 2007Nationwide• Bio-Logic Systems Corp

Steris Corp: Steris QFC1728 and QFC1729 Quick Connects used in connect...

The center insert of the adaptor #6 restrictor could become loose and/or come out of the housing and may affect the sterilization process of the attached endoscope

FDAFeb 23, 2007CA, CO, ID +12 more• Steris Corp

Beckman Coulter Inc: FP1000 Cell Preparation System Software versions 1.1 & 1....

Pressure (from recapped tubes) or vacuum (from under-filled short-draw tubes) will cause inaccurate results if not properly vented.

FDAFeb 22, 2007Nationwide• Beckman Coulter Inc

Joerns Healthcare Inc.: Sunrise Medical-Hoyer Advance Patient Lifts (Portable and...

Unapproved Design Change (by base supplier) consisting of a reduction in the number of mast-to-base welds (from four welds to two welds).

FDAFeb 21, 2007AL, AK, AZ +42 more• Joerns Healthcare Inc.

1...3197 319831993200 3201...3411

Page 3199 of 3411Next