toddler product Recalls

Fagron Compounding Services Norepinephrine Bitartrate Injection Recall Affects 5,140 Bags (2026)

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

Teva Octreotide Acetate Injectable Suspension Recall 21,930 Cartons Over Sterility Risk (2026)

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

Curosurf 240 mg Poractant Alfa Recalled for Sterility Concerns (2026)

Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.

Pure Vitamins and Natural Supplements Boner Bears Honey Recall for Undeclared Sildenafil and Tadalaf

FDA analysis revealed the presence of undeclared sildenafil and Tadalafil

Brahms PlGF Plus KRYPTOR 859075N Recall Expands to 5,254 Units Worldwide (2026)

Stryker Sustainability Solutions Color Cuff Recall Expands to 56,740 Cuffs Over Detachment Risk (202

Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)

Lack of Assurance of Sterility

Fresenius Kabi 5% Dextrose Injection Recalled for Lack of Sterility Assurance (2026)

Lack of Assurance of Sterility

Cook Medical Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled Over Expired-Lot

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Arterial Pressure Monitoring Tray Recalled Over Expired Shelf-Life Labeling (Z-1778-202

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set for Expired-

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Spectrum Central Venous Tray Recalled Over Expired Shelf-Life Labels (2026)

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical CTO-6 Micro Wire Guide Recalled Worldwide Over Expired Shelf Life Labels (2026)

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Tornier Tornier HRS Max Parts Recalled for Mislabeling, Incompatibility (2026)

Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.

Cook Medical Blue Rhino G2-Multi Tracheostomy Introducer Set Recalled for Expiration Date Labeling —

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Multipurpose Drainage Catheter Recalled Over Expired Labeling in Lots G29775

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set Recall Affects 484 Units (Z

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical NCompass Nitinol Stone Extractor Recalled Over Expiration Date Shelf-Life Concerns (202

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Approach CTO-12 Micro Wire Guide Recall Affects 49 Units for Expired Shelf-Life Labels

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Spectrum Central Venous Catheter Tray Recalled for Expired Shelf Life Labels (2026)

Cook Medical recalled 1,872 units of Spectrum Central Venous Catheter Trays worldwide due to expiration dates labeling that exceed true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions."