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Quality Electrodynamics Llc

Quality Electrodynamics Llc Recalls

All product recalls associated with Quality Electrodynamics Llc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 17541–17560 of 21320 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.

Boston Scientific Corp: Soft Tip Sheath Multipurpose Introducing Sheath Kit, Mode...

The marker band may detach from the sheath and a clinical failure could result in an embolism.

FDA

1...876 877878879 880...1066

Page 878 of 1066Next

Dec 24, 2008

Nationwide

• Boston Scientific Corp

Boston Scientific Corporation: Gold Probe 10FR Working Length: 300 cm, Probe Tip O.D. 3....

Packaging tray for the Gold Probe Single-Use BiPolar Electrohemostasis Catheters may have a crack. Cracks in the tray or damage to the tray of the Gold Probe device may lead to a compromised sterile barrier.

FDADec 24, 2008Nationwide• Boston Scientific Corporation

Boston Scientific Corp: Convoy Advanced Delivery Sheath Kit, Model Numbers: M00...

The marker band may detach from the sheath and a clinical failure could result in an embolism.

FDADec 24, 2008Nationwide• Boston Scientific Corp

Boston Scientific Corporation: Gold Probe 7FR Working Length: 300 cm, Probe Tip O.D. 2.3...

FDADec 24, 2008Nationwide• Boston Scientific Corporation

Depuy Orthopaedics, Inc.: DePuy DNP Anatomic Fracture Repair System, Locking Screw ...

The DNP nail plate may not attach to the alignment guide (jig) instrument, making it difficult to insert the nail plate into position or to drill needed holes accurately.

FDADec 23, 2008Nationwide• Depuy Orthopaedics, Inc.

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

Siemens Medical Solutions USA, Inc: Artiste MV Digital Linear Accelerator System Equipped wit...

The range of tolerance is to high for the accessory holder, therefore, Wedges and other accessories do not latch to the locking mechanism correctly.

FDADec 20, 2008Nationwide• Siemens Medical Solutions USA, Inc

Stryker Howmedica Osteonics Corp.: Triathlon X3 Posterior Stabilized Tibial Insert Use with ...

Stryker Orthopaedics became aware of a lot for lot mix-up between part numbers 5532-G-713, lot code LBD528 (Triathlon X3 Posterior Stabilized Tibial Insert, size 7-13 mm) and part 5532-G-813, lot code LBD512 (Triathlon X3 Posterior Stabilized Tibial Insert Size 8-13 mm)

FDADec 18, 2008Nationwide• Stryker Howmedica Osteonics Corp.

Siemens Medical Solutions USA, Inc.: Siemens Medical Solutions E.CAM Patient Handling System (...

Patient fingers can get pinched if they attempt to pull themselves up from the patient handling system without any assistance and grabbing onto the flip-up FOV indicator bars.

FDADec 18, 2008Nationwide• Siemens Medical Solutions USA, Inc.

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

Commercial Frozen Food Merchandisers (Tyler) – Fire Hazard (2008)

Fire/Burn Risk

The recalled Vertical Multi-deck Frozen Food Merchandisers are typically used in grocery stores and other commercial settings. The recall involves models D6F, D6FL, L6F, L6FL, N6F and N6FL manufactured between 1995 and 2008. The serial and model numbers are located on the label located on the inside, upper-right front of the unit behind the lighting assembly. A complete list of the serial numbers involved in this recall can be found at www.tylerrefrigeration.com

CPSCDec 11, 2008Nationwide• Tyler Refrigeration, of Niles, Mich.

Philips Medical Systems North America Co. Phillips: Allura XPER 10/10

Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.

FDADec 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Integris Allura Flat Detector 9C

Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.

FDADec 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Integris H5000F

Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.

FDADec 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips