292 recalls tagged with “toddler product”.
Fagron Compounding Services recalled 5,140 bags of norepinephrine Bitartrate injection due to lack of sterility assurance. A blue Break-Off-Part could detach from the administration port. The recall covers nationwide distribution in the U.S. Consumers should stop use and contact providers for guidance.
Teva Pharmaceuticals recalled 21,930 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the United States. The recall stems from lack of assurance of sterility identified during an FDA inspection at the contract manufacturer. Healthcare providers and patients should stop using this product immediately and contact Teva or a physician for guidance.
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.
FDA analysis found undeclared sildenafil and tadalafil in Boner Bears Honey 100% Wildflower Honey. The recall covers 15-pouch boxes manufactured in Florida with distribution in New Jersey. Consumers should stop using the product and seek refund or replacement from Pure Vitamins and Natural Supplements.
Brahms GmbH recalled 5,254 units of the PlGF Plus KRYPTOR in vitro diagnostic test worldwide after reports of QC values out of range at QC Level 1. The issue may cause falsely elevated sFlt-1/PlGF ratios and higher risk classifications for preeclampsia progression. Stop using the device immediately and follow manufacturer recall instructions.
Stryker Sustainability Solutions recalled 56,740 color cuff tourniquet cuffs due to potential detachment from the bladder. The recall affects 18" and 24" cuffs across multiple U.S. states. Patients and healthcare providers should stop using these devices immediately and follow manufacturer instructions.
Fresenius Kabi USA recalled saline injections distributed nationwide, including Alaska and Puerto Rico. The action covers multiple batch numbers with sterility concerns. Healthcare providers and patients should stop using the product immediately and follow official guidance for replacement options.
Fresenius Kabi USA, LLC recalls 5% Dextrose Injection, USP 12.5 g per 250 mL in FreeFlex bags due to lack of sterility assurance. The recall covers units distributed nationwide including Alaska and Puerto Rico. Healthcare providers and patients should stop use and consult a healthcare professional.
Cook Incorporated recalled 441 units of the Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray after identifying expiration dates that exceed true shelf life. The recall covers lots with Reference Part Numbers C-PTISY-100-HC-G-NA, C-PTISY-100-UNL-HC-G-NA and C-PTISY-100-UNS-HC-G-NA distributed worldwide. Healthcare providers must stop use and follow manufacturer recall instructions.
Cook Medical recalled 20 arterial pressure monitoring trays worldwide after labeling showed expiration dates that exceeded true shelf life. The recall targets two reference part numbers, APMY-2.5-15-0-2.5 and APMY-4.0-21J-1-12. Healthcare providers should stop using affected lots immediately and follow recall instructions.
Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set after lots were labeled with expiration dates that exceed true shelf life. The recall affects two reference parts with multiple UDI and lot numbers. Healthcare facilities should stop use and follow recall instructions.
Cook Medical recalled 2,348 Spectrum Central Venous Tray units worldwide due to expiration dates that exceed true shelf life. The recall affects lots labeled with overstated expiration dates. Healthcare providers and patients should stop using the affected devices and follow manufacturer instructions.
Cook Medical recalled 15 CTO-6 Micro Wire Guides sold worldwide after labeling errors extended expiration dates beyond true shelf life. The devices carry Reference Part Number CMW-14-190-6G and Order Number G50786. Healthcare providers were notified to stop use immediately until further instructions.
Tornier recalls 233 surgical parts nationwide in the United States. The items were mislabelled as Tornier HRS Max products. These parts fit the Tornier HRS system only and are incompatible with the Tornier HRS Max system. Clinicians and patients should stop using the affected parts and follow recall instructions.
Cook Medical recalled 916 units of the Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set worldwide after discovering expiration dates exceeded true shelf life. The recall affects multiple reference part numbers and order numbers. Healthcare providers should stop using the device immediately and follow Cook’s instructions for recall notification.
Cook Incorporated recalled 20 units of its Multipurpose Drainage Catheter reference ULT8.5-38-25-P-CLMS-8-RH-FS distributed worldwide. The recall cites expiration dates that exceed the product’s true shelf life. Healthcare providers and patients should stop using the affected devices immediately.
Cook Incorporated recalls 484 Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Sets due to expiration date labeling that exceeds true shelf life. The recall is active and distributed worldwide. Health care providers must stop use and follow recall instructions.
Cook Medical recalled 70 NCompass nitinol stone extractors worldwide after labeling showed expiration dates that exceed their true shelf life. The recall affects lots labeled C-NTSE-2.4-115-NC3 (G36250) and C-NTSE-2.4-115-NCT4 (G36251). The company classifies the action as Class II and says the issue could affect patient safety.
Cook Medical recalled 49 units of the Approach CTO-12 Micro Wire Guide due to expiration dates that exceed the true shelf life. The recall covers two reference part numbers and multiple lots distributed worldwide. Healthcare providers and patients should stop using the affected devices immediately. Follow the manufacturer’s recall instructions or contact a healthcare provider for guidance.
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."