Argon Medical is correcting affected convenience kits by removing included Spectra Medical Devices Lidocaine Ampules. 

July 24, 2026 – Shirley, NY, American Regent, Inc. is conducting a nationwide voluntary recall of a single lot of Papaverine Hydrochloride Injection, USP, 60 mg/2 mL single dose vial to the consumer level. The product is being recalled due to the presence of particulate matter identified as glass an

July 24, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling Lot LD175708, Exp 14-Feb 2027 of Cefazolin in Dextrose Injection due to a report of particulate matter found in the solution identified as cardboard.Risk Statement: The use of the defective product has a

July 24, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling Lot LD175708, Exp 14-Feb 2027 of Cefazolin in Dextrose Injection due to a report of particulate matter found in the solution identified as cardboard.
Risk Statement: The use of the defective product has a

ENROUTE Transcarotid Neuroprotection Systems may have arterial sheath tip separation or partial tip separation during use

July 24, 2026 - Taoyuan City, Taiwan - Sunny Pharmtech, Inc is voluntarily recalling three lots of Cyclophosphamide for Injection, USP, 1g/vial and 2g/vial, to the User Level due to the presence of particulate matter identified as steel. To date, no adverse events or injuries associated with this pa

FOR IMMEDIATE RELEASE – July 18th, 2026 – Panoli, Gujarat, Unique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.) is voluntarily recalling four lots of Cetirizine Hydrochloride Tablets USP 5 mg to the consumer level due to cross contamination with Ranitidine.

Baxter administration sets may have air bubbles in the drip chamber and tubing, which may result in air being delivered through the IV line to the patient.

Prolonged use of the Abiomed 14Fr Low Profile Introducer may lead to thrombus formation.

Saline, Lidocaine and Bupivacaine from affected convenience kits should not be used.

B. Braun is removing affected convenience kits containing recalled Bupivacaine Hydrochloride in Dextrose Injection components

Failure of an electrical component in certain Astral ventilators may cause an interruption or failure in therapy which may result in serious injury or death

Volara system patient circuits may leak air and medication from the nebulizer cup during therapy, leading to reduced oxygenation and ineffective nebulization.

The distal tip in certain lots of the Medtronic Harmony Delivery Catheter System (DCS) may detach which can require endovascular retrieval or surgical intervention.

Certain BD ChloraPrep Applicators in Convenience Kits manufactured by Medline may not be sterile. 

A software anomaly may cause a false battery-health value. The pump should remain plugged in at all times.

If dropped, the Ivenix pump touchscreen may become unresponsive and should be removed from use.

Certain Cardinal Health Webcol Large Alcohol Prep Pads in Custom Convenience Kits manufactured by Aligned Medical Solutions are not sterile.

Specific Impella CP Sets are out of specification; use may result in low purge pressure events from the onset of the case

Certain Omnipod Pods may have a tear in the tubing that allows insulin to leak outside the Pod instead of being delivered to the body.