Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,093–1,104 of 1,121 recalls
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Hydration issue resulting in the product being less cohesive and moldable than intended due to an issue with the polymer.
Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products.