Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–12 of 49 recalls
Test manufactured with an expired ingredient which may present as either a false negative or positive.
Test manufactured with an expired ingredient which may present as either a false negative or positive.
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility.…
Product does not have FDA clearance.
Cribs sold in the USA are missing two access door warning labels.
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Butyrate tube cracks during actuation, rendering product unusable.
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together.…
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together.…