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 ↗

RSS Feed

Home
/
Brands
/
Quality Electrodynamics Llc

Quality Electrodynamics Llc Recalls

All product recalls associated with Quality Electrodynamics Llc.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

582

Class I (Serious)

Most Recent

Dec 2025

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 9141–9160 of 10937 recalls

Quality Electrodynamics Llc: Mirror assembly to magnetic resonance device (1.5T Atlas ...

The firm received a complaint indicating that the mirror is high risk and could drop on a patient.

FDADec 29, 2008Nationwide• Quality Electrodynamics Llc

Philips Healthcare Informatics, Inc.: iSite PACS (Picture Archiving and Communications System) ...

Product may display clinical reports with the study date and time in GMT format, which may not be obvious to the end user, who may expect to see the local time in the report.

FDADec 29, 2008Nationwide• Philips Healthcare Informatics, Inc.

Bicycle Suspension Forks (Magura) – Crash Hazard (2008)

The suspension fork is located on the bicycle's front wheel. They are white or black. "Magura" and "MD100R" or "MD80R" are printed on the forks.

1...456 457458459 460...547

Page 458 of 547Next

CPSC

Dec 23, 2008

Nationwide

• Gustav Magenwirth GmbH & Co. KH, of Germany

Alpine Ski Bindings (Atomic) – Unexpected Release (2008)

The recall affects the heel components of the following Atomic alpine ski bindings: Race 310, Race 412, RaceRace 310, RaceRace 412, Xentrix 310, Xentrix 311, Xentrix 412, C310, C311, C412, CR 310, CR 412, R 310, R 412, SX 310, SX 412, Device 311, Device 412, Centro 310, Centro 412, and Dynamic ADX 312, RD10, X412, Centro 412. The recall includes only those bindings manufactured from 1998 through 2002 The year of manufacture can be located on the underside of the heel lever.

CPSCDec 23, 2008Nationwide• Atomic Skis GmbH, of Austria

Philips Medical Systems North America Co. Phillips: PCR Eleva. The marketing brochure is labeled in parts: "...

There is a risk of selecting the wrong patient, when patient is selected in the patient list and the examination tab pressed with background query are running at the same time.

FDADec 23, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Smiths Medical PM, Inc. N7: Smiths Medical BCI(R) Advisor(R) Vital Signs Monitor, mod...

Recent improvements were made to the Advisor case plastic resulting in the inserts being deeply embedded into the plastic. This affects the ability of the monitor to be adequately secured on the wall mount bracket or roll stand bracket, resulting in the monitor falling off. There have been no adverse events or injuries reported.

FDADec 22, 2008FL, GA, NJ +2 more• Smiths Medical PM, Inc. N7

Majestic High Chairs (Evenflo) – Fall Risk (2008)

Choking Hazard

The recall involves Evenflo Majestic™ high chairs made before January 23, 2007. The recalled high chairs have the following model numbers: 3001395A, 3001583, 3001633A, 3001669, 3001700A, 3001713, 3001713A, 3001730A, 3001732, 3001732A, 3001733, 3001742, 3001742A, and 3001756. The model number and production date can be found on a white label on the seatback. "Evenflo" is printed on the label and on the push button on the front of the tray.

CPSCDec 18, 2008Nationwide• Evenflo Company Inc., of Miamisburg, Ohio

Migada Inc. P.O Box 888 Kiryat Shmona Israel: TEVADAPTOR Closed Drug Reconstitution and Transfer System...

Syringe adaptor is disintegrating when attached to the end of the syringe.

FDADec 18, 2008Nationwide• Migada Inc. P.O Box 888 Kiryat Shmona Israel

Smiths Medical MD, Inc.: Smiths Medical Medfusion Model 3500 Syringe Infusion Pump...

Delay in therapy. Keypad issues with Medfusion Syringe Infusion Pump, model numbers 3500-306 and 3500-415 ("Pump") have occurred during implementation or shortly after first being placed into use. These issues can be intermittent, and may render the Pump inoperable or the Pump may not respond to certain keypad button presses.

FDADec 18, 2008Nationwide• Smiths Medical MD, Inc.

Mountain Cat Snowmobiles (Arctic Cat) – Fire Hazard (2008)

Fire/Burn Risk

This recall involves all 2009 model Mountain Cat and Crossfire snowmobiles within the Vin number range of 103896 through 118441. The Vin number can be found stamped into the tunnel near the right-side footrest.

CPSCDec 16, 2008Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Newport Medical Instruments Inc: Newport e360 Ventilator, Rx only. The e360 Ventilator S...

In December 2008, Newport initiated a field correction to upgrade e360 ventilators with software versions 3.0 or higher to software version 3.3. As a result of this upgrade, some customers experienced unexpected device alert alarms. Newport's investigation into these complaints confirmed that the 3.3 software responds too quickly to certain situations, giving a false device alert. Newport condu

FDADec 15, 2008AL, AZ, CA +20 more• Newport Medical Instruments Inc