Wyoming recalls

Some BD Alaris Pump Module 8100 infusion pumps have a software date/time issue related to daylight saving time that may prevent them from connecting to hospital networks. This affects only the network connectivity function; the pump's ability to deliver medication is not impacted. The issue involves 189 devices distributed in Arizona, Indiana, Ohio, and Virginia.

Philips SmartPath to dStream MR imaging systems with software versions R11.1 and R12.1 may display incorrect stiffness values when MR Elastography maps are exported to a PACS viewer. This could affect the accuracy of tissue stiffness measurements used for clinical assessment. Three units have been identified worldwide.

Philips dStream 3.0T MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when elastography images are sent to picture archiving systems (PACS). This affects the accuracy of tissue stiffness measurements used in clinical diagnosis.

Philips MR 7700 MRI systems running software versions R11.1 or R12.1 may display incorrect stiffness values when MR Elastography images are exported to a PACS viewer. This could affect the accuracy of tissue stiffness measurements used in clinical evaluation.

Philips MR 7700 MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when elastography maps are exported to medical imaging viewing systems. This affects 9 units worldwide. No injuries have been reported.

Philips Ingenia Elition X MRI systems with certain software versions (R11.1 and R12.1) may display incorrect stiffness values when MR elastography maps are exported to a PACS viewer. This could lead to misinterpretation of tissue stiffness measurements used in clinical diagnosis.

Philips Ingenia Elition S MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when MR Elastography maps are exported to a PACS (Picture Archiving and Communication System). This could affect the accuracy of tissue stiffness measurements used in clinical evaluation. Five units worldwide have been identified.

Philips has identified a potential error in how stiffness values are displayed when MR Elastography (MRE) images are exported to a PACS viewer on certain Ingenia Ambition X MRI systems. This affects 21 systems worldwide running software versions R11.1 or R12.1. The error could result in incorrect stiffness measurements being shown to clinicians.

Philips has recalled certain Ingenia Ambition S. MRI systems (software versions R11.1 and R12.1) because they may display incorrect stiffness values when MR Elastography images are sent to a PACS (picture viewing system). This could affect the accuracy of medical imaging data used for diagnosis.

Philips has recalled certain Ingenia 3.0T CX MRI systems (software versions R11.1 and R12.1) because stiffness values displayed in exported elastography maps may be inaccurate when viewed in a PACS (Picture Archiving and Communication System). This affects 6 units worldwide, primarily in the United States and Europe.

Philips has identified a software issue in certain Ingenia 3.0T MRI systems that may cause incorrect stiffness values to appear when viewing elastography images on a PACS (picture viewing system). This affects 24 systems worldwide with specific software versions. No injuries have been reported.

Philips has recalled certain Ingenia 1.5T MRI systems with software versions R11.1 and R12.1. When MR Elastography stiffness maps are exported to a PACS viewer, the stiffness values may display incorrectly. This could affect the accuracy of diagnostic information viewed in those systems.

Philips MR systems (Evolution Upgrade 3.0T, software versions R11.1 and R12.1) may display incorrect stiffness values when MR Elastography maps are exported to a PACS viewer system. This could affect the accuracy of imaging data used in clinical assessment.

Philips Evolution Upgrade 1.5T MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when elastography maps are exported to a PACS viewer. This could affect the accuracy of tissue stiffness measurements used in clinical diagnosis. Three units have been identified worldwide.

Cardinal Health is updating instructions for multiple chest drainage unit models to clarify they are intended only for adults 18 years and older. When used on infants, these devices may not show proper bubbling or fluid movement, which can make it hard for clinicians to tell if the device is working correctly. This could delay or prevent needed treatment.

The touchscreen on certain Zimmer A.T.S. 3200TS tourniquet systems may freeze or stop responding when the device is set to operate in certain non-English languages. This could delay surgery while staff locate an alternate device. The issue affects systems running software version 2.06 or earlier.

The screen on Zimmer A.T.S. 5000TS Tourniquet Systems may freeze or stop responding when used in certain non-English language settings. This can delay surgery while staff locate an alternate device. The issue affects systems running software version v2.04 or earlier.

Medline medical procedure convenience kits containing MASTISOL liquid adhesive were recalled because the tubing can crack when the adhesive vial is opened. This could prevent proper use of the adhesive during surgery. No injuries have been reported.

Medline distributed three types of medical procedure kits containing MASTISOL liquid adhesive where the tubing can crack when the vial is opened. This could prevent proper adhesive application during cesarean section procedures. No injuries have been reported.

Medline distributed circumcision procedure kits (SKU DYNJ16826O) that contained MASTISOL liquid adhesive with a manufacturing defect. The tubing on the adhesive vials can crack when opened, which could affect the sterility and usability of the adhesive during the procedure.

Medline distributed medical procedure convenience kits containing MASTISOL liquid adhesive with a manufacturing defect. The adhesive vials have butyrate tubing that can crack when opened, potentially compromising the adhesive's sterility and usability during procedures.

Medline distributed six types of neurosurgery procedure convenience kits containing MASTISOL liquid adhesive. The tubing in the adhesive vials can crack when opened, which may compromise the sterility or usability of the kit. No injuries have been reported.

Medline medical procedure convenience kits containing MASTISOL liquid adhesive were distributed with a manufacturing defect. The butyrate tubing in the adhesive applicator vials can crack when used, potentially affecting the adhesive's delivery or safety during medical procedures.

Medline medical procedure convenience kits (SKU P903933B) contain MASTISOL liquid adhesive with defective tubing that can crack when the vial is used. The cracked tubing could prevent proper product delivery during medical procedures.

Medline distributed 66 different medical procedure kits containing MASTISOL liquid adhesive with defective butyrate tubing that can crack when the vial is opened. The adhesive is used to secure medical devices during surgical procedures. No injuries have been reported.

Medline distributed eight types of medical procedure convenience kits that contained MASTISOL liquid adhesive with a manufacturing defect. The tubing in the adhesive vials can crack when opened, which could affect the sterility or usability of the kit during medical procedures.

Medline distributed 30 types of surgical procedure convenience kits that contained MASTISOL liquid adhesive with a manufacturing defect. The tubing on the adhesive vials can crack when opened, potentially affecting the sterility of the kit. About 456 affected kits were distributed; no injuries have been reported.

Medline distributed nine types of medical procedure convenience kits containing MASTISOL liquid adhesive. The adhesive vials have defective tubing that can crack when used, potentially compromising the sterility and function of the kits. About 40 units were affected.

Medline distributed three medical procedure convenience kits containing MASTISOL liquid adhesive with a defect: the tubing can crack when the adhesive vial is opened. This affects breast-hernia-port, breast biopsy, and dermatology procedure kits. No injuries have been reported.

Medline distributed eight types of medical procedure convenience kits containing MASTISOL liquid adhesive. The adhesive vials had cracked butyrate tubing that could break when the vial is opened, potentially affecting the sterility or usability of the kit.