Medline Industries, LP recalled 596 medical convenience kits on July 25, 2025. The recall affects kits with Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to light failure. Patients and healthcare providers must stop using these devices immediately.
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.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
The recall includes the following kits: 1. Newborn Resuscitation Kit, Kit Number ACC010381C; 2. Drawer 5 - Position 3, Kit Number ACC010532; 3. Drawer #4C Adult, Kit Number ACC010671; 4. Drawer #2, Kit Number ACC010728. These kits were distributed in Alabama, California, Delaware, Oregon, Tennessee, and Texas.
The recalled kits contain laryngoscope handles that may fail to illuminate. This failure could hinder critical medical procedures requiring proper visualization.
No injuries or incidents related to this issue have been reported so far. The recall is classified as Class I, indicating a high risk.
Patients and healthcare providers should stop using the recalled kits immediately. Contact Medline Industries, LP or your healthcare provider for detailed instructions on the recall.
For more information, contact Medline Industries, LP at their Northfield location or visit their website.
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.