2,228 recalls tagged with “stop use immediately”.
GE Healthcare recalled 364 Omni Legend systems on December 24, 2025, after reports of image quality issues. The recall affects multiple models distributed worldwide, including the Omni Legend 16 and 21. Users should stop using the devices immediately due to potential diagnostic inaccuracies.
Medline Industries, LP recalled 7,570 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks with an open seal risk. Healthcare providers and patients should stop using these kits immediately.
Zimmer Surgical recalled 51 A.T.S. 3200TS Tourniquet Systems on December 24, 2025, due to a malfunctioning user interface. The device may freeze or become unresponsive in non-English language settings, risking delays in emergency situations. Healthcare providers should stop using the device immediately and follow recall instructions.
Medline Industries, LP recalled 130 Intubation Trays on December 24, 2025. The recalled trays may contain a smaller suction catheter that could cause respiratory failure. Patients and healthcare providers should stop using the device immediately.
Medline Industries, LP recalled 141,971 suction catheter kits on December 24, 2025. The kits may contain a smaller catheter that can lead to serious respiratory issues. Health providers and patients must stop using the kits immediately to prevent potential harm.
Medline Industries, LP recalled 2,448 Suture Removal Trays on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potentially open seals. The company urges immediate cessation of use to avoid potential hazards.
Medline Industries, LP announced a recall of 216 kits packaged as Sterile Resection Packs on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks that may have an open seal. The recall affects healthcare providers and patients nationwide.
Medline Industries, LP recalled 21,854 medical kits on December 24, 2025, due to potential packaging defects. The recall affects kits containing BD ChloraPrep Triple Swabsticks with compromised seals. Patients and healthcare providers must stop using these kits immediately.
Zimmer Surgical Inc recalled 206 A.T.S. 5000TS Tourniquet Systems on December 24, 2025. The device can freeze or become unresponsive in certain non-English language settings. This issue may delay patient care during emergencies.
Medline Industries, LP recalled 4,300 blood culture kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with packaging that may exhibit an open seal. This defect poses a high risk to patient safety.
Medline Industries, LP recalled 1,350 medical convenience kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potential open seals. Users should cease using these kits immediately and follow manufacturer instructions for return.
Medline Industries, LP recalled 8,445 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks which may have an open seal. This defect poses a high risk to patients and healthcare providers.
Medline Industries, LP recalled 120 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks with potentially open seals. This recall affects products distributed nationwide in the U.S.
Medline Industries, LP recalled 7,380 medical convenience kits on December 24, 2025. The recall affects the PowerGlide Dressing Change Kit and Central Line Tray with ChloraPrep swabsticks. An open seal on packaging may compromise sterility and patient safety.
Focalyx Technologies issued a recall for its Focalyx Fusion software device on December 23, 2025. The device may malfunction with Windows 10, potentially causing patient harm during prostate biopsies. Users must stop using the device immediately until it is validated with Windows 11.
Willy Pete's Chocolates recalled 54 units of Almond Despair dark chocolate on December 22, 2025. The product contains undeclared almonds which pose a risk to consumers with nut allergies. Customers should stop using the product and seek a refund or replacement.
LSL Healthcare recalled 1,400 Central Line Dressing Kits on December 22, 2025. BD ChloraPrep Triple Swabsticks in these kits have open seals on their packaging. This defect poses a serious risk during medical procedures.
DPT Laboratories recalled 92,376 tubes of Diclofenac Sodium Topical Gel, 1%, on December 22, 2025. The recall is due to the product failing pH specifications, posing a high risk to consumers. Users should stop using the gel immediately and contact healthcare providers for guidance.
Medline Industries recalled reprocessed St. Jude electrophysiology catheters on December 22, 2025. The recall affects 48 units potentially contaminated with residual materials. The defective catheters pose a high risk of inflammation and systemic infection.
Medline Industries recalled 511 reprocessed AcuNav ultrasound catheters on December 22, 2025. These devices may contain small particles that can cause serious health risks such as systemic infections and embolisms. Healthcare providers must stop using the affected devices immediately to prevent potentially life-threatening complications.