205 recalls tagged with “laceration risk”.
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Lack of Assurance of Sterility
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Joyreal recalled busy board toys on February 26, 2026, due to choking and laceration hazards. The toys can have small parts that pose serious risks to children. Consumers must stop using these toys immediately and seek refunds.
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
Olympus Corporation of the Americas recalled 326 PKS Cutting Forceps worldwide. The devices may have welding defects that cause the jaw to break during use. Stop using the device immediately and follow the recall instructions provided by Olympus.
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
Products may be contaminated with Listeria monocytogenes.
Products may be contaminated with Listeria monocytogenes.