95,114 total recalls in our database
Teleflex Medical
The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
Possible leak from the filter allowing a small of amount of air to be released from the junction between the filter end cap (flat side of the filter) and the filter housing connection.
The connection between the beeper subassembly and the pump may fail. The GemStar infusion pump will identify this failure during the "self-test" while powering up which will result in a Beeper Error ("code 10/001/000"). This Beeper Error (code 10/001/000) is a service alarm that places the pump in an inoperable mode and requires service before it can be returned to service.
Hospira MedNet 5.5, 5.8.1, and 5.8.2 contains software defect where the dosing units of "nanog/kg/min" and "milliUnits/min" are not sent to a Plum A+ device (Version 13.40, 13.41, and 13.4.2) via Auto Programming when those dosing units are not properly established in the customized drug library. A dosing unit mismatch of "nanog/kg/min" or "milliUnits/min" on an unmatched medication will produce a
The Aquatec¿ Fixed Backrest withstands a load of only 250 newtons at uneven load. This may result in the Fixed Backrest becoming detached from the frame.
B. Braun Medical
Complaints were received that reported the stopcock of some Stopcock Extension Sets are assembled in the reverse position, resulting in the stopcock being closed when set in the open position and vise versa.
3M Company - Health Care Business
Labeling on units shipped prior to May 16th, 2014 did not contain the statement "This product contains dry natural rubber" as required by the United States Food and Drug Administration (FDA) for medical devices. The non-slip pads at the bottom of the unit contain dry natural rubber. One incident of an allergic reaction in a sensitized individual has been reported.
Teleflex Medical
The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
Intuitive Surgical
Patient Side Cart battery boxes may overheat in rare charging conditions, causing battery bulging.
Teleflex Medical
The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
STERIS has identified that deformation of the washers door handle pin may occur when the door handle is rotated with sufficient force. Should deformation and/or breakage of the door handle pin occur there is a potential for the washer door to become inoperable.
Teleflex Medical
The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
Terumo Cardiovascular Systems
An evaluation of the APS1 Operator Manual found that existing instructions lack clarity and accuracy related to specific items.
Vascular Technology
Report of the product penetrating the sterile barrier; this could render the product unsterile.
Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Aesculap Inc. (AIC (USA)) has initiated a voluntary recall of Dafilon Black 10/0 (0.2) 15 cm DRm4 non-sterile non-absorbable polyamide Surgical Suture due to a labeling issue. Box labels do state non-sterile; however there is an additional label that is affixed on the box that states the product is sterile.
Teleflex Medical
The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
Vascular Technology
Report of the product penetrating the sterile barrier; this could render the product unsterile.
Teleflex Medical
The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
RGI Medical Manufacturing
Problem with low adhesion of the tubing to luer connection which may lead to a separation of the extension set while in use.