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BD has identified internally that the infusion sets contain di(2-ethylhexyl) phthalate (DEHP) and have not been labeled accordingly. Recall start date: November 13, 2023

In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…

Per the VITROS CKMB slides instructions for use (IFU) "principles of the procedure" section, the spread layer of the CKMB slide contains goat antihuman CK-mm antibodies, which inhibit CK-mm (muscle) activity and ~50% of the CK-mb (heart) activity. The…

The manufacturer of the NIV angled mouthpiece with Notch 22F/15F, advised that devices in lots 32304444, 32305269 and 32306017 were produced with unintended open slits on the side of the mouthpiece body. This allows some of the respiratory gas to escape…

BD has identified internally that the infusion sets contain di(2-ethylhexyl) phthalate (DEHP) and have not been labeled accordingly. Recall Start Date: October 12, 2023

In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…

Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iviewgt™ / xvi detector arms. when the detector arm is fully deployed there is no risk of uncontrolled…

Unomedical A/S has found that in rare cases the VariSoft infusion set connector detaches more easily from the infusion set than expected, requiring less force to disconnect than intended, thereby interrupting the delivery of insulin. Recall start date…

CHS initiated this recall after receiving a recall letter from Baxter which stated that: "This action is being taken as a precautionary measure as there may be a potential for leaking or dislodged membrane ports on the solution bags during the spiking…

Resmed's Astral ventilator is designed to deliver a Total Power Failure (TPF) audible alarm for at least 2 minutes to alert the carer/clinician when the ventilator experiences a total loss of power that results in a stop of ventilation. The TPF audible…

Specific lots of Cardinal Health Monoject™ luer-lock tip syringes (6 and 35 ml) have demonstrated recognition and compatibility issues with certain syringe infusion pumps. As a result, Cardinal Health recommends that they not be used with syringe…

Venue Go standard carts may have an internal failure of the vertical/horizontal tilt adjustment mechanism. Recall Start Date: September 19, 2023

Olympus found that certain lots of the CV-190 do not start up properly and as a result, the image from the endoscope is not displayed when the operations listed below are performed because parts that deviated from the specification were assembled into…

The shaft and tip component of the Universal Joint Screwdriver was manufactured with the incorrect raw stainless steel material. Recall start date: September 1, 2023

Siemens Healthcare will be informing customers about potential dot- or line-shaped artifacts caused by the presence of lubricating grease within the headband of the over-ear headphones listed below when used during head examinations with the Magnetom MRI…