Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged with the incorrect size device (GVL 1 Stat (blades)).
Other Medical Devices
π₯ Medical Devices β’ 15,809 recalls
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
Ferno PROFlexxΒΏ Model 28Z Chair Cot
Ferno-Washington
The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.
Artis zee, Angiographic x-ray system
Siemens Medical Solutions USA
Software error - As a result of a software fault in Artis zee systems with software version VD11 and an A100 generator, the possibility exists that following the failure of a tube assembly focus, the Artis system functions properly until the next reactivation. Following reactivation, the system no longer initializes as intended.
Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room, which could lead to damage to the system and potentially cause thermal events such as a burning odor, smoke or fire.
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
Hemotherm CE, model 400CE, Heater-Cooling Device
Cincinnati Sub-Zero Products
Improperly rated fuses were used in the manufacture of the device.
The On/Off functionality in the LCSU 4 is controlled by electronic components, one of which might be damaged.
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090
Signal Medical
Potential for poly tip of the mallet to come off during use. Potential for foreign material in the surgical field or delay in surgery. Reminder for customers that the poly tip must be removed for cleaning and sterilization to assure proper cleaning and sterilization of the entire mallet.
Alcon is initiating a Voluntary Medical Device Removal because the product supplier has stated that there is potential for sterile packaging to be compromised.
UNIQ: UNIQ FD10 722026; UNIQ FD10/10 722027; UNIQ FD20/10 biplane 722029; UNIQ FD10 OR Table 722033; UNIQ FD10/10 OR Table 722034; UNIQ FD20/10 OR Table 722036; UNIQ FD20/20 722038; UNIQ FD20/20 biplane OR Table 722039
Philips Electronics North America
Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room, which could lead to damage to the system and potentially cause thermal events such as a burning odor, smoke or fire.
Merge Eye Station and Merge Eye Care PACS.
Merge Healthcare
During an antivirus program scan of the Eye Station or Eye Care PACS, the antivirus program may detect a newly captured image to be an unwanted file and delete the image permanently.
The tensile strength minimum as directed by USP <881> was not met over the length of the product's shelf life.
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming