🦴

Implants & Prosthetics

πŸ₯ Medical Devices β€’ 4,540 recalls

Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter heart valve crimper because they may not open sufficiently when the handle is rotated in the full open position. As a result, user may have difficulty fitting a 26mm Sapien transcatheter heart valve into the crimper orifice when preparing the valve for crimping.

Jan 20, 2014 Implants & Prosthetics Nationwide View Details β†’

Siemens Healthcare Diagnostics confirmed customer complaints regarding an increase in the number of euthyroid patients (those with normal function of the thyroid) demonstrating values above the recommended normal range as published in the Instructions For Use for the IMMULITE/IMMULITE 1000 and/or IMMULITE 2000/IMMULITE 2000 XPi for several lots of Free T3 kits. A positive bias in quality control results was also observed, but the values may remain within the established ranges.

Aug 27, 2013 Implants & Prosthetics Nationwide View Details β†’

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

May 16, 2013 Implants & Prosthetics Nationwide View Details β†’

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

May 16, 2013 Implants & Prosthetics Nationwide View Details β†’

Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Number H965450140, Catalog Number 45-014; 2) 8F/SL/Titanium Ports/NF, Product Number H965450170, Catalog Number 45-017; 3) 6F/SL/Plastic Port/F, Product Number H965450200, Catalog Number 45-020; 4) 8F/SL/Plastic Port/F, Product Number H965450220, Catalog Number 45-022; 5) 8F/SL/Titanium Ports/F, Product Number H965450250, Catalog Number 45-025; 6) Plastic/6F/non-filled/non-valved, Product Number H965450290, Catalog Number 45-029; 7) Plastic/6F/filled/non-valved, Product Number H965450300, Catalog Number 45-030; 8) Plastic/8F/non-filled/non-valved, Product Number H965450310, Catalog Number 45-031; 9) Plastic/8F/filled/non-valved, Product Number H965450320, Catalog Number 45-032; 10) Plastic/6F/non-filled/valved, Product Number H965450370, Catalog Number 45-037; 11) Plastic/6F/filled/valved, Product Number H965450380, Catalog Number 45-038; 12) Plastic/8F/non-filled/valved, Product Number H965450390, Catalog Number 45-039; 13) Plastic/8F/filled/valved, Product Number H965450400, Catalog Number 45-040; 14) Titanium/6F/non-filled/valved, Product Number H965450410, Catalog Number 45-041; 15) Titanium/8F/non-filled/valved, Product Number H965450430, Catalog Number 45-043. Product Usage: ***K-Shield Port Access Infusion Set, (affected product) supplied by Kawasumi Laboratories. The K-Shield Port Access Infusion Set with High Pressure Tubing is an intravascular administration set with a non-coring Huber needle that is used to access an implanted medication port for solution infusion. This device is also indicated for injection of contrast media by a power injector only with power injectable implanted port.***NMI Port is indicated for patients who require long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.

Navilyst Medical

Class I - Dangerous

Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a possible breach of sterilization barrier.

Nov 25, 2013 Implants & Prosthetics Nationwide View Details β†’

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

May 16, 2013 Implants & Prosthetics Nationwide View Details β†’

The unit displays an error code of hose kinking when no hose kink is present; the unit fails to monitor the temperature of the water in the blanket as intended and controlling it through the automatic temperature control. This failure could result in temperature injuries to the treatment site; and there have been two reports of electric shock.

Sep 17, 2013 Implants & Prosthetics Nationwide View Details β†’

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

May 16, 2013 Implants & Prosthetics Nationwide View Details β†’

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

May 16, 2013 Implants & Prosthetics Nationwide View Details β†’

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

May 16, 2013 Implants & Prosthetics Nationwide View Details β†’

The unit displays an error code of hose kinking when no hose kink is present; the unit fails to monitor the temperature of the water in the blanket as intended and controlling it through the automatic temperature control. This failure could result in temperature injuries to the treatment site; and there have been two reports of electric shock.

Sep 17, 2013 Implants & Prosthetics Nationwide View Details β†’

The unit displays an error code of hose kinking when no hose kink is present; the unit fails to monitor the temperature of the water in the blanket as intended and controlling it through the automatic temperature control. This failure could result in temperature injuries to the treatment site; and there have been two reports of electric shock.

Sep 17, 2013 Implants & Prosthetics Nationwide View Details β†’

The ACUTE Innovations Ribloc U plus Rib Fracture Plating System is recalled because it has the potential to malfunction during installation in a surgery.

Oct 30, 2013 Implants & Prosthetics View Details β†’

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

May 16, 2013 Implants & Prosthetics Nationwide View Details β†’

Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single Lumen Broviac Catheter because a small number of Silicone catheters in the may be undersized to 5.3 Fr instead of 6.6 Fr as stated in the labeling for the device.

Dec 6, 2013 Implants & Prosthetics Nationwide View Details β†’

A defect in the controller board can lead to the condenser to the video monitor becoming too warm. This could potentially cause the video monitor to shut off.

Apr 16, 2013 Implants & Prosthetics Nationwide View Details β†’

Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single Lumen Broviac Catheter because a small number of Silicone catheters in the may be undersized to 5.3 Fr instead of 6.6 Fr as stated in the labeling for the device.

Dec 6, 2013 Implants & Prosthetics Nationwide View Details β†’

The patient label associated with the product may be incorrect in that the lot number on the patient label may be different than the lot number on the outer carton label.

Nov 4, 2013 Implants & Prosthetics Nationwide View Details β†’