inforMED
InjuryBZW

MON-A-THERM

Received Apr 23, 2008 · Event occurred Sep 1, 2007

Report 2936999-2008-00186 · MDR key 1033372

Device

Generic name

Esophageal Stethoscope W/temp

Model number

EST18FR

Catalog number

90042

Product problems

  • Unknown (for use when the device problem is not known)

Patient

45 YR

  • Laceration(s) of Esophagus
  • Surgical procedure aborted/stopped
  • Surgical procedure, additional

Narrative

Description of Event or Problem

DURING A REQUEST FOR PRODUCT INFO THE CALLER STATED THAT IN 2007 A STAFF CRNA WAS DOING A CASE CERVICAL DISCECTOMY. THEY NOTICED THE TIP OF THE PROBE IN THE SURGICAL SPACE. THE CASE WAS DISCONTINUED AND A THORACIC SURGEON CAME IN AND STATED THERE WAS A LINEAR TEAR IN THE ESOPHAGUS AND REPAIRED THE TEAR. CERVICAL AREA WAS CLOSED AND PT RETURNED TO FLOOR. THE CALLER STATED PT IS DOING FINE AND PT HAD COMPLETED DISCECTOMY IN LATER SURGERY.

Additional Manufacturer Narrative

REPEATED CALLS HAVE BEEN MADE TO THE HOSPITAL TO GAIN FURTHER INFO INCLUDING A LOT NUMBER AND TO DETERMINE IF THIS INCIDENT WAS PREVIOUSLY REPORTED BY OTHER STAFF MEMBER(S) IN 2007. IN 2007, A SIMILAR CALL WAS RECEIVED FROM AN ANESTHESIA NURSE REPORTING TO BE FROM THE SAME HOSPITAL. THE NURSE REPORTED THE END USER (A SURGEON) WAS WORKING IN THE SAME AREA AS THE ESOPHAGUS DURING AN OPERATIVE PROCEDURE. DURING THE PROCEDURE THE PT DEVELOPED A PERFORATION OF THE ESOPHAGUS, HOWEVER, IT WAS NOT CAUSED BY THE ESOPHAGEAL STETHOSCOPE. NO OTHER INFO WAS PROVIDED. FOLLOW-UP CALLS WERE MADE TO THE HOSPITAL AND WE REQUESTED THE ESOPHAGEAL STETHOSCOPE BE RETURNED FOR OUR EVAL. NO DEVICE WAS RETURNED. A LOT NUMBER WAS PROVIDED AND THE MFR'S REVIEW FOUND NO NONCONFORMANCE FOR THE LOT. IN RESPONSE TO THIS RECENT CALL, WE MADE SEVERAL ATTEMPTS TO CONTACT THE HOSPITAL ANESTHESIA AND RISK MANAGEMENT AND THERE HAS BEEN NO RESPONSE. ALTHOUGH AT THIS TIME WITHOUT A LOT NUMBER, OR ADD'L INFO FROM STAFF WE CAN NOT BE ABSOLUTELY CERTAIN THIS RECENT REPORTED INFO IS A DUPLICATE, HOWEVER, WE BELIEVE IT IS. IF WE RECEIVED ANY NEW SIGNIFICANT INFO FROM THE HOSPITAL, OR THE DEVICE IS RETURNED FOR OUR INVESTIGATION, A FOLLOW-UP REPORT WILL BE SUBMITTED.