95,083 total recalls in our database
Medtronic Neuromodulation
Medtronic received a complaint that there was an error code displayed on the programmer when the physician attempted to interrogate an implanted SynchroMed II pump. The error code prevented the physician from updating the pump; however the pump was providing therapy.
Resource Optimization & Innovation
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Resource Optimization & Innovation
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Ion Beam Applications S.A.
The Proton Therapy System can allow gantry rotation even if the snout is not properly locked.
Resource Optimization & Innovation
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Resource Optimization & Innovation
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Resource Optimization & Innovation
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Focus Diagnostics
After a submission for CLIA database update from Focus Diagnostics to DiaSorin Molecular,the company found that their Legionella IFA device (IF0950) is not 510(k) exempt.
Resource Optimization & Innovation
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Resource Optimization & Innovation
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Unknown Manufacturer
The zipper pull can detach from the sweatshirt, posing choking and laceration hazards to children.
Unknown Manufacturer
The recalled chests are unstable if they are not anchored to the wall, posing a serious tip-over and entrapment hazard that can result in death or injuries to children. The chests do not comply with the performance requirements of the U.S. voluntary industry standard (ASTM F2057-14).
Rexon Industrial Corp., Ltd. of Taiwan
The table saw stand can collapse unexpectedly, posing laceration and impact injury hazards to the operator.
Unknown Manufacturer
The bottom of the glass dressing shaker bottle can break when the metal agitator strikes the glass bottom, posing a laceration hazard.
Unknown Manufacturer
The capCAP can leak, dislodge or come off, posing a burn hazard to consumers when the bottles are used to hold hot liquids.
Unknown Manufacturer
The button on the top of the infant cap can detach, posing a choking hazard.
Manzana Products Co.
Manzana Products Co. is initiating a recall of three varieties of apple sauce after receiving customer complaints or finding small pieces of glass in the product.
Sargento Foods
Sargento Foods Inc. was notified by their supplier that the cheese that was supplied may have been contaminated with Listeria monocytogenes.
Ciao Bovina
Ciao Bovina, LLC announces a voluntary field action for Italian Strawberry Gelato due to potential contamination with Hepatitis A Virus.
During sanitation, the firm discovered metal pieces missing from a sifter screen.