Missouri recalls

Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Certain lots of product have the potential for a sterile barrier breach.

Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to procedural delay and/or the need to select an alternative implant.

Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption with the potential for the patient to receive less infusion solution than intended. Exposure of hazardous substances to the patient, caregiver, or pharmacy technician is possible.

Affected devices exhibited fractures at the distal shaft tip without complete detachment.

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

potential presence of Salmonella

potential presence of Salmonella

potential presence of Salmonella

potential presence of Salmonella

potential presence of Salmonella

potential presence of Salmonella

Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Foreign object: black particulate matter