Monitor U.S. medical device recall enforcement reports from the FDA. Review product descriptions, recall reasons, classifications, dates, recalling firms and distribution information where the FDA provides them.
27,110 detailed records are currently available in this category.
The set screw is not able to advance or reverse from the original position in the nail.
Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
Monopolar Curved Scissor (MCS) instruments may be susceptible to developing cracks near the proximal edge of the extension tube. These cracks may fracture the plastic surrounding the…
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The secure filesystem client software used in the interface between the Vidistar PACS and an EHR system may cause intermixed images from multiple patients showing in a single study.
The torque wrench used on the ceiling column assembly during a recent service visit was outside of the torque specification, potentially overtightening the bolts. The overtightening of…
The Quality Control Certificate for certain AutoDELFIA Neonatal IRT Kits is missing information required to assess the acceptability of measured control values which may result in a delay…
A size 22mm threaded peg was found in the package of a 10mm unit.
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
Medical device recall records can change as the FDA receives additional information. Check the official record identifier and current FDA information before making health or product-use decisions.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.
