Applied Medical Technology recalled 1,780 NutraGlide Nasal Feeding Tubes on August 12, 2025, after reports of distal tips detaching. This recall affects tubes distributed in Massachusetts and Rhode Island. The detachment poses a high risk for patients requiring enteral nutrition.
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Applied Medical Technology Inc or your healthcare provider for instructions. Notification method: Letter
The recall includes NutraGlide Nasal Feeding Tubes with Stylet and ENFit, sizes 5 F - 6 F x 55, REF E NRT-05055-I. These tubes were distributed in the US, specifically in Massachusetts and Rhode Island.
The distal tips of the NutraGlide Nasal Feeding Tubes may detach at lower than expected forces. This defect poses a significant risk to patients who depend on these feeding tubes for nutrition, fluids, and medications.
There have been no reported injuries or incidents associated with this recall. The potential for detachment remains a serious concern for patient safety.
Patients and healthcare providers should stop using the NutraGlide Nasal Feeding Tubes immediately. Follow the recall instructions provided by Applied Medical Technology Inc. Contact the manufacturer or your healthcare provider for further instructions.
For more information, contact Applied Medical Technology Inc. at [insert phone number]. Additional details can be found on their website or through the FDA recall notice.
Abiomed issued a recall for 10,153 Automated Impella Controllers on October 1, 2025. The devices face potential cybersecurity vulnerabilities related to their operating system. Healthcare providers and patients should stop using these devices immediately.
Acuity Specialty Products recalled its Wyandotte Sanifect E3 hand sanitizer on September 29, 2025. The recall affects multiple package configurations due to potential methanol contamination. Consumers should stop using the product immediately and contact the company for guidance.
AFCO recalled hand sanitizer on September 29, 2025, due to a risk of methanol contamination. The company failed to conduct required testing on incoming alcohol components. Consumers should stop using the product immediately.