All Recalls

95,094 total recalls in our database

The firm received two customer complaints local Pelton & Crane distributors that the Helios 3000 track mounted dental lights were missing the two 8/32x3/16 set screws during the initial installation of the dental light.

Mar 8, 2016 Other Medical Devices Nationwide View Details →

ICU Medical has identified an issue with a connection in an isolated number of I.V. infusion administration sets that incorporate the ChemLock additive port. In these sets, the connection between the Drip Chamber or Bag Spike and the ChemoLock port has the potential for developing a leak.

Feb 25, 2016 Infusion Pumps Nationwide View Details →

ICU Medical has identified an issue with a connection in an isolated number of I.V. infusion administration sets that incorporate the ChemLock additive port. In these sets, the connection between the Drip Chamber or Bag Spike and the ChemoLock port has the potential for developing a leak.

Feb 25, 2016 Infusion Pumps Nationwide View Details →

In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect Gantry angle for the first beam of an IMRT treatment if certain specific conditions are met. If Gantry angle for the first beam of IMRT is incorrectly set and if nobody is aware of it, an erroneous treatment would be given to the patient.

Mar 7, 2016 Other Medical Devices Nationwide View Details →

Due to the risk of a recently identified cross reactivity, the Elecsys Estradiol assay should not be used when monitoring patient being treated with fulvestrant. Customers should be informed that fulvestrant will increase the apparent concentration of estradiol in women being treated with this drug. If treatment with fulvestrant has been altered or discontinued as a result of falsely elevated e

Mar 7, 2016 Infusion Pumps Nationwide View Details →

Foot Switches used with the following systems: Philips Allura Xper Systems; 722001 AlluraXperFDlO C, 722002 Allura Xper FD1O F, 722003 Allura Xper FD1O, 722005 Allura Xper FD1O/10, 722006 Allura Xper FD2O, 722008 Allura Xper FD2O Biplane, 722010 Allura Xper FD1O, 722011 Allura Xper FD1O/10, 722012 Allura Xper FD2O, 722013 Allura XPER FD2O BIPLANE, 722014 Allura Xper FD1O OR Table, 722015 Allura Xper FD2O OR Table, 722019 Allura Xper FD1O/10 OR Table, 722020 Allura Xper FD2O Biplane OR Table, 722022 Allura Xper FD1O OR Table, 722023 Allura Xper FD2O OR Table, 722024 Allura Xper FD1O/10 OR Table, 722025 Allura Xper FD2O Biplane OR Table, 722026 Allura Xper FD1O, 722027 Allura Xper FD1O/10, 722028 Allura Xper FD2O, 722029 Allura Xper FD2O/10, 722031 Allura CV2O, 722033 Allura Xper FD1O OR Table, 722034 Allura Xper FD1O/10 OR Table, 722035 Allura Xper FD2O OR Table, 722036 Allura Xper FD2O/10 OR Table, 722038 Allura Xper FD2O/20, 722039 Allura Xper FD2O/20 OR Table, 722058 Allura Xper FD20115, 722059 Allura Xper FD2O/15 OR Table, 722123 Field extensions Xper cardio systems, 722124 Field extensions Xper vascular systems, 722126 SmartPath to AlluraClarity cardio, 722127 SmartPath to AlluraClarity vascular, 722133 Field ext. Xper cardio systems R7.6, 722134 Field ext. Xper vascular systems R7.6, 722400 Cardio Vascular-Allura Centron, 889006 Diamond Select Allura Xper FD1 0 The Allura Xper FD Series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. Tis included, e.g., peripheral, cerebral, thoracic and abdominal angiography, as well as PTAs, stent placements, embolisations and thrombolysis. Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as PTCA, stent placing, atherectomies), pacemaker implantations, and electrophysiology (EP). Non-vascular interventions such as drainages, biopsies and vertebroplasties procedures. Additionally: The Allura Xper FD series is compatible with a hybrid Operating Room. FD10 is compatible with specific magnetic navigation systems

Philips Medical Systems

🏥 Medical Devices Class I - Dangerous

Loss of key image functionality due to a bent pedal of the Footswitch.

Sep 24, 2014 Implants & Prosthetics Nationwide View Details →

Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve Gray, NecLoc Extrication Collar, Rebound Cartilage, Rebound Cartilage Custom, Rebound Air Walker, Rebound Diabetic Walker, Back Support Suspenders Clip on Black, Back Support Suspenders Sew On Black, Extreme Custom, Unloader Custom XT, Unloader Custom Lite, Unloader Custom, and Papoose Infant Spine Immobilizers because the p

Feb 24, 2016 Implants & Prosthetics Nationwide View Details →

The anterior/posterior (AP) dimension may be oversized by 0.016. If the femoral component does not fit as tightly as intended, bony ingrowth may not occur causing loosening of the femoral component. A revision surgery may be necessary.

Feb 5, 2016 Implants & Prosthetics View Details →

Due to a leak in the cooling system, fluids could potentially seep into the equipment cabinet. Loss of coolant can result in a cooling system failure and subsequent system failure. This leak can occur sporadically in affected systems.

Feb 18, 2016 Diagnostic Equipment Nationwide View Details →

ICU Medical has identified an issue with a connection in an isolated number of I.V. infusion administration sets that incorporate the ChemLock additive port. In these sets, the connection between the Drip Chamber or Bag Spike and the ChemoLock port has the potential for developing a leak.

Feb 25, 2016 Infusion Pumps Nationwide View Details →

Women's Scarves

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

The scarves do not meet the federal flammability standards for clothing textiles, posing a burn risk.

Apr 6, 2016 Other Consumer Products Nationwide View Details →

Mattresses

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

All Niposul and NipoFlorida Elegance, Elegance Gold, and Evolution mattresses fail to meet the mandatory federal open flame standard for mattresses.

Apr 6, 2016 Other Consumer Products Nationwide View Details →

Children's loungewear

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

The loungewear fails to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.

Apr 5, 2016 Children's Products Nationwide View Details →

Givenchy men's silk T-shirts

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

The T-shirts fail to meet the federal flammability standard for wearing apparel and pose a risk of burn injury to consumers.

Apr 5, 2016 Clothing & Accessories Nationwide View Details →

KUL fan heaters

Unknown Manufacturer

🏠 Consumer Products Class I - Dangerous

The fan heaters can overheat, posing a fire hazard.

Mar 31, 2016 Furniture Nationwide View Details →

Children's footed pajamas

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

The pajamas fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.

Mar 31, 2016 Children's Products Nationwide View Details →

Nestle is recalling a limited number of DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.

Mar 10, 2016 Produce Nationwide View Details →