inforMED
MalfunctionCBL

*

Received Nov 6, 2000 · Event occurred Oct 1, 2000

Report 9616692-2000-00002 · MDR key 304371

Device

Generic name

*

Model number

*

Catalog number

12344

Product problems

  • False Device Output

Patient

Not reported

  • Unknown (for use when the patient's condition is not known)

Remedial action

  • Other