495 recalls tagged with “suffocation risk”.
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.
Yiruikeji2024 recalled magnetic chess games on February 24, 2026, due to ingestion hazards. The games contain loose magnets that can pose serious health risks to children. Consumers should stop using the product and seek a refund immediately.
SAMIT recalled multi-purpose helmets for children on February 19, 2026. The helmets fail to meet safety standards, posing a risk of serious injury or death. Consumers should stop using them immediately and seek a refund.
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.
Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*) pumps.
Probes may rupture/burst during activation