Overview of recall records associated with Applied Medical Resources Corp, including dates, categories and classifications where available.
Classification mix: Class II: 19, Class I: 3.
Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.
Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.
There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
The firm has received reports of tip separation during usage of the catheters, which may expose patients to unintended dislodgement of the tip from the body of the catheter.
The firm has received reports of tip separation during usage of the catheters, which may expose patients to unintended dislodgement of the tip from the body of the catheter.
The firm has received reports of tip separation during usage of the catheters, which may expose patients to unintended dislodgement of the tip from the body of the catheter.
Unintentional shifting of the tip insulation of the firm's electrosurgical probes.
Unintentional shifting of the tip insulation of the firm's electrosurgical probes.
The product may not have met sterility requirements . Use of a non-sterile device on a patient may expose the patient to infectious agents.
Increased customer complaints indicating inconsistent clip application; may lead to unoccluded vessels.
Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260,…
Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260,…
Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260,…
Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260,…
Potential to improperly characterize tissue within the jaws, which may result in nonoptimal power delivery.
This page summarizes recall records in which the official source identifies Applied Medical Resources Corp as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
