Every recall we track for DIXI MEDICAL USA — 9 in all — plus the complaints and injury reports the public filed about them.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have specific UDI codes. Consumers should contact for details.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have UDI:0366453:000138. Stop using if packaging may be damaged.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have UDI:0366453:14. Stop using if packaging may be damaged.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have specific UDI codes; contact for remedy.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have UDI: 03664:03664539000053. Stop using if packaging may be deformed.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have UDI:0366453:000091. Stop using if packaging may be deformed.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have UDI:0366453:000152. Stop using if packaging may be deformed.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have UDI 036645390:000077. Stop using if packaging may be damaged.
DIXI Medical recalls Microdeep Depth Electrodes due to potential packaging deformation that could compromise sterile barrier. Affected units have UDI:0366453:000176. Stop using if packaging may be deformed.
