1,862 recalls tagged with “stop use immediately”.
Medline Industries has recalled 3,578,805 units of its sterile saline wound wash due to potential sterility assurance issues. The recall, effective January 5, 2026, affects products distributed worldwide, including in the U.S. Consumers should stop using the product immediately.
Medline Industries recalled 104,608 units of sterile saline wound wash on January 5, 2026. The product may not have met the required sterility assurance level. Consumers should stop using this product immediately and follow recall instructions.
Medline Industries recalled 10,550 wound care kits on January 5, 2026, due to potential sterility issues. The recall affects several model numbers, including DYKM1361A and DYKM2013. Consumers should stop using the kits immediately and follow the manufacturer's instructions.
Medline Industries recalled 1,640 units of its Nail Kit, Model POD14214, on January 5, 2026. The recall stems from concerns that the sterile saline wound wash may not meet required sterility standards. Patients and healthcare providers must stop using the product immediately.
Medline Industries recalled 8,773 units of its Nail Kit, Model Number DYKM1528, on January 5, 2026. The recall stems from a failure to meet required sterility assurance levels in the saline wound wash. Patients and healthcare providers should stop using the product immediately.
AVID Medical recalled 1,500 units of the TRANSPORT BAG KIT on January 2, 2026. A seal issue with the Tyvek bag may compromise the sterility of the kit. The recall affects healthcare providers and patients in New Jersey.
Alphatec Spine recalled 7 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The incorrect navigated array connection geometry poses a high hazard risk in surgical settings. Healthcare providers and patients must stop using the devices immediately.
Alphatec Spine recalled 15 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The navigated array connection geometry is incorrect, posing risks during surgical procedures. Healthcare providers and patients should stop using the instruments immediately.
Toyota recalled certain 2021-2025 Sienna Hybrid vehicles on January 2, 2026. The recall affects vehicles with improperly tightened seatback bolts. This issue increases the risk of injury during a crash.
Cipla USA, Inc. is recalling 15,221 Lanreotide Acetate Injection syringes nationwide in the United States after detecting particulate matter. The defect is the presence of particulate matter in the injectable solution. Healthcare providers and patients should stop using the product immediately and contact Cipla USA for guidance.
Kia America, Inc. is recalling 2025 Sorento Hybrid vehicles due to a software error. The issue may cause a loss of low beam headlights and taillights. Owner notifications were mailed on February 21, 2025.
BioGlo Fluorescein Sodium Ophthalmic Strips are recalled due to sterility issues. The recall affects 184,320 containers distributed nationwide in the USA. Consumers should stop using the product immediately.
Wizcure Pharmaa recalled 17,280 cartons of Vista Gel Hypromellose eye drops on December 31, 2025. The recall stems from a lack of assurance of sterility, raising potential health risks for users. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
Medline Industries recalled over 926,000 IV Administration and Extension Sets due to a significant risk of leaks and breaks. The recall affects multiple models with potential exposure to chemicals and mechanical forces. Users should discontinue use immediately to prevent serious health risks including blood loss and infections.
Miach Orthopaedics recalled 284 units of the BEAR Implant, Model Number 1000, on December 31, 2025. The recall stems from an incorrect expiration date on the label that exceeds the product's approved shelf life. Patients and healthcare providers should stop using the device immediately and follow recall instructions.
Wizcure Pharmaa Pvt. Ltd. recalled 139,104 cartons of Vista Gonio Eye Lubricant on December 31, 2025. The recall stems from a lack of assurance of sterility due to non-compliance with manufacturing practices. Consumers are urged to stop using the product immediately and seek guidance from healthcare providers.
Wizcure Pharmaa recalled 10,080 boxes of Fluorescein Sodium Ophthalmic Strips on December 31, 2025, due to sterility issues. The recall affects products packaged in 100-count and 300-count boxes. Consumers should stop using these products immediately and consult healthcare providers for guidance.
Wizcure Pharmaa recalled 50,400 boxes of Bio Glo Fluorescein Sodium Ophthalmic Strips on December 31, 2025. The recall follows concerns regarding lack of assurance of sterility, as products did not conform to good manufacturing practices. Consumers should stop using the product immediately and consult healthcare providers.
Wizcure Pharmaa recalled 5,760 cartons of Vista Tears Eye Drops on December 31, 2025. The recall follows a lack of assurance of sterility in the product. Consumers should stop using the drops immediately and contact a healthcare provider for guidance.
Zydus Pharmaceuticals recalled 22,896 bottles of Icosapent Ethyl capsules on December 30, 2025. The recall stems from leakage and oxidation that may reduce the drug's effectiveness. Consumers should stop using the product immediately and seek guidance from healthcare providers.