Home / Recalls / Medical Devices
DeRoyal Industries Inc recalls DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02
Recalled December 21, 2022 · FDA recall Z-0707-2023 · DeRoyal Industries
Hazard
XXX · FDA Class II
Units
336 kits
Sold at
US: Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts, Arizona, Missouri, Connecticut, New Jersey, Pennsylvania, North Carolina, Louisiana, Michigan, Minnesota, Ohio, Indiana, Kansas, Illinois, Alabama, Georgia, Mississippi
Description
XXX
Product
DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02
Manufacturer(s)
DeRoyal Industries Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →