STERIS has learned that groups of LED lights (modules) contained within the vLED light head may illuminate inconsistently.
Medical Devices Recalls
Medical equipment, implants, and diagnostic devices
KCI has received reports that, in a small number of cases, the CelluTome Harvester (a component of the CelluTome Epidermal Harvesting System), blades have the potential to drift during shipping and could prematurely protrude into openings of harvester top plate.
Cervical Extension Machine for Physical Therapy
MedX Holdings
Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.
There is the potential for a breach in the inner or outer packaging pouches of all lots of the Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle.
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
There are additional and updated warning and cautions that are not in the Patient At-Home Guide for HomeChoice Automated PD Systems and HomeChoice PRO Automated PD Systems.
Siemens Medical Solutions USA, Inc. has received reports of unintended radial motion of the detectors. This unintended motion, should it occur, may cause the patient compression related injuries.
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
An ECG procedure time stamp is incorrect, due to a software error in the McKesson Cardiology ECG Management with software versions 13.1 and 13.1.1.
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
Intuitive Surgical is initiating a voluntary correction related to da Vinci Si System (IS3000) Vision Side Carts, with threaded-in caster wheels, which can result in the caster wheel bolts gradually unthreading and the wheels loosening.
An increase in complaint trending for a loss of audible sound associated with the timer has been observed.
Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis.
Baxter Healthcare
System error 01779 is produced when the battery cannot be charged due to specific voltage differences between the battery and the charger.
ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006) have broken and produced small pieces. Should a fracture occur and not be observed during surgery, there is the potential for these small fractured pieces of the instrument to be left in the patient.
Dimension Vista Myoglobin Calibrator (MYO CAL), Lot 4FD085 Product usage: in vitro diagnostic product for the calibration of Myoglobin (MYO) method on the Dimension Vista System.
Siemens Healthcare Diagnostics
Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift in MYO QC and Patient test results that exceeds acceptance criteria for this product. A positive shift observed up to 12% at MYO concentrations within and above the reference range of the assay. Depending on quality control limits, this drift may not be detected.
Use of excessive force when impacting may lead to intra-operative femoral fracture.
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
The device may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start. Unintended start of the hand piece or wrong mode/direction could cause bone/soft tissue, peripheral nerve, and /or vascular damage. Injuries may need surgical or medical intervention. Surgical delay and postoperative local infection are also potential risks.