Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
NAMIC Fluid Management Convenience Kits contains a Fluid Delivery Set that was not assembled in accordance with specification, and prevents the device from being used, resulting in a minor…
Potential risk for helium gas inside the MR examination room during a magnet quench
Potential risk for helium gas inside the MR examination room during a magnet quench
Bags of solution may have a small leak at the base of the injection port where the port is welded into the body of the bag..
Potential risk for helium gas inside the MR examination room during a magnet quench
Closing the Emergency Stop may disable the horizontal motor, allowing the couch top to move during patient load or unload activities.
The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB) Catheter was missing the Contraindications section.
The temperature of the incubation lids of the MINC Bench top Incubators may become too high or too low for proper gamete/embryo incubation due to fatigue failure of the flat flex lid heater.
Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex Connector may become loose or disconnect before use or during use.
Surview scan with tube current lower than 30 mA is unable to be initialized.
The UDI label correctly reads IBR12d-13, however, the inner label incorrectly read IBNT12d-13.
The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB) Catheter was missing the Contraindications section.
Data has shown that degradation of a raw material used in Phantom Fiber may occur more quickly than expected if improperly stored. This may impact the shelf-life of the product which could…
Potential risk for helium gas inside the MR examination room during a magnet quench
The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB) Catheter was missing the Contraindications section.
Update to cooler-heater cleaning instructions.
Closing the Emergency Stop may disable the horizontal motor, allowing the couch top to move during patient load or unload activities.
The integrity of the sterile packaging is potentially compromised.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Pump was found to be constructed from crimp connectors that do not meet the fixation wiring requirements and can cause failure of the device to operate or electric shock or burn to the user.
potential Allergen cross contact in oil used to roast various nuts and seeds products.
Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.
potential Allergen cross contact in oil used to roast various nuts and seeds products.
potential Allergen cross contact in oil used to roast various nuts and seeds products.
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