DC recalls

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Due to incorrect incubation process being performed on product.

Due to incorrect incubation process being performed on product.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-lock leaks during manipulation of the frangible and tubing when preparing the product for use for treatment. This issue presents the potential of a slip and fall hazard associated with fluid on the floor.

Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.

The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.