Health & Personal Care Recalls

Medline Recalled 7,913 Reprocessed ACUSON AcuNav Ultrasound Catheters for Intracardiac Imaging

Medline Reprocesses 7,913 Electrophysiology Catheters for Safety Risks

Medline Recalls 7,913 Reprocessed ViewFlex Xtra ICE Catheters for Particulates (2025 Recall)

Medline Livewire Steerable EP Catheters Recalled for Particulates in 2025 (7,913 Units)

Exela Pharma Sciences 4.2% Sodium Bicarbonate Injection Recalled Over Arsenic Impurity Out-Of-Spec

Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.

Fortress Introducer Sheath System 386594 Recall Expanded; 2,500 Units Worldwide Distribution (High-R

Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.

Over 4,300 S.I.N. Implant EPIKUT Dental Implants Recalled Due to Quality Concerns

Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which could compromise product quality and performance.

Pfizer Levoxyl Recall: Subpotent Levoxyl 50 mcg Tablets, 29,004 Bottles in U.S. Market (2025)

Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.

Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems

Ortho-Clinical Diagnostics Recalls 2,320 VITROS LAC Slides for Calibration Failures on XT Systems (W

Sucralfate Tablets Recall Expanded After CGMP Deviations; 26,992 Blister Packs Affected

Ortoma AB Recalls 261 Inserter Adapters for Hip Cup Tools (2025)

Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

Medline Recalls 2,520 Kits With Flexicare Laryngoscope Handles Over Lighting Failure (2025)

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.

Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Medline Recalls 596 Flexicare BritePro Solo Fiber Optic Laryngoscope Handles in 2025

Medline Industries, LP recalled 596 Medline kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light may fail to illuminate as designed. Healthcare providers should stop using the devices immediately and follow recall instructions.

Merit Medical 10Fore Hemostasis Valve Recalled Due to Foreign Body Risk

Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.

Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)

Due to incorrect/lack of Unique Device Identifier (UDI) codes.

Zap Surgical Systems ZAP-X Radiosurgery System Recalled for 17 Units Worldwide in 2025

Cipla USA Albuterol Sulfate Inhalation Aerosol Recall Expanded for Stability Variance (2025)

Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point.

Beckman Coulter MicroScan Neg MIC 56 Panels Recalled for Contamination Risk (2026)

Due to the likely presence of contamination in well(s).