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 ↗

Home
/
Brands
/
Rita Medical Systems, Inc.

Rita Medical Systems, Inc. Recalls

All product recalls associated with Rita Medical Systems, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 23201–23220 of 25000 recalls

Rita Medical Systems, Inc.: RITA Starburst MRI SemiFlex (3-5 cm Diameter/25cm Length)...

The product may have a cracked tray which can compromise the sterility of the product.

FDAApr 3, 2007Nationwide• Rita Medical Systems, Inc.

Groovy Grabber Bracelets (A&A Global) – Lead Poisoning (2007)

The recalled bracelets are made of flexible metal bands wrapped in decorative plastic covers. The bracelets come in various colors and designs, including smiley faces, Chinese symbols, dogs, cats, aliens, checker boards, and flames.

CPSCApr 3, 2007Nationwide• A&A Global Industries, of Cockeysville, Md.

GE OEC Medical Systems, Inc: Radiological Image Processing System The system is an ai...

The FluoroTrak Spinal Navigation Application on the OEC 9900 EliteNAV could result in an incorrect position of the navigated instrument(s) versus the displayed reference image.

1...1159 116011611162 1163...1250

Page 1161 of 1250Next

FDA

Apr 2, 2007

FL, IL, IN +6 more

• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: Radiological Image Processing System The system is an ...

The FluoroTrak Spinal Navigation Application on the OEC 9900 EliteNAV could result in an incorrect position of the navigated instrument(s) versus the displayed reference image.

FDAApr 2, 2007FL, IL, IN +6 more• GE OEC Medical Systems, Inc

Wako Chemicals USA, Inc.: NEFA Standard Solution Calibrator, Oleic Acid, 1 mmol/L, ...

Diagnostic reagent for clinical laboratory testing was incorrectly labeled.

FDAMar 30, 2007Nationwide• Wako Chemicals USA, Inc.

Hamilton Co: Microlab F.A.M.E. reagent containers, Part number 148482,...

Some product containers may be leaking.

FDAMar 29, 2007IN, NJ, TX +1 more• Hamilton Co

Binax, Inc. dba IMPD: BinaxNOW A&B Kit 10 Test Kit (Japan) Part No. 416-110J ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Binax, Inc. dba IMPD: BinaxNOW Influenza A&B 22 Test Kit Part Number: 416-022, ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Binax, Inc. dba IMPD: BinaxNOW Nasopharyngeal (NP) Accessory Pak, Part Number 4...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Binax, Inc. dba IMPD: BinaxNOW Influenza A&B 10 Test KIT Part Number: 416-110 ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Binax, Inc. dba IMPD: BinaxNOW RSV 10 Test Kit Part Number : 430-100, contains ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

GE OEC Medical Systems, Inc: OEC 9800 Plus Digital; MDL number A349855. Product Usage...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC MiniView 6800 Mobile; MDL number A349855. Product ...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 Plus Digital; MDL number A349855. Product Usa...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: UroView 2800; MDL number A349855. Product Usage: Designe...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: UroView 2800; MDL number A349855. Product Usage: Desig...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC MiniView 6800 Mobile; MDL number A349855. Product Us...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

General Electric Med Systems LLC: GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic ...

Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patient contouring. Usage of Innova Sense patient contouring for such devices could potentially lead to patient injury.

FDAMar 26, 2007Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 4100/4100 IQ. Digital Fluoroscopic ...

Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function on Innova Digital (located in control room) or in-room InnovaCentral/Touch-Screen

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging...

Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patient contouring. Usage of Innova Sense patient contouring for such devices could potentially lead to patient injury.

FDAMar 26, 2007Nationwide• General Electric Med Systems LLC