RUSCH MALLONEY FR28F, P/N9213 MEDICAL UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00 report with the FDA on 2015-01-16 for RUSCH MALLONEY FR28F, P/N9213 MEDICAL UNKNOWN manufactured by Teleflex Medical.

Event Text Entries

[5420745] Alleged event: issue occurred in (b)(6) where the patient/plaintiff was undergoing laparoscopic bariatric surgery in which there was a need to pass an orogastric tube through the esophagus into the stomach, but difficulty was encountered in attempting to pass the tube. A bougie was passed into the stomach successfully, but even this did not make the tube pass through the esophagus. So, the surgeon attempted to laparoscopically attach a suture to the end of the bougie so that the suture could be pulled out through the patient's esophagus with removal of the bougie, then attached to the orogastric tube to pull the orogastric tube back into the stomach. The surgeon did not realize that the bougie contained mercury, and the procedure resulted in some mercury being released into the patient's abdomen. The attorney for the surgeon indicated that the patient did not suffer any significant ill effects. There was a (b)(6) 2011) submitted that reported the same event: pt scheduled for laparoscopic roux-en-y procedure. Difficult placement of ng tube requiring placement of bougie dilator to assist in naso-gastric insertion which was the final phase of the operative procedure to assure no evidence of leak. Bougie was a rusch hurst style manufactured prior to 2003. Bougie was modified to assist in the insertion of the nasogastric tube. A suture was placed through one end of the dilator with a tail of suture material attached. It was discovered that the suture had apparently punctured the liner lumen of the dilator, allowing mercy to escape outside of the dilator. Event was reported by a risk manager. The (b)(4) report stated a rusch hurst style but the brand name was listed as a rusch malloney fr28f. No contact information was provided.
Patient Sequence No: 1, Text Type: D, B5


[12762916] Qn # (b)(4). A complaint history review was conducted on the catalog number in question from 01/05/2010 to 01/06/2015. Since the catalog number is unknown it cannot be related to any complaint for same catalog number and same issue. The device sample is not expected for investigation since the event was received from medwatch. The manufacturer will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004365956-2015-00016
MDR Report Key4432978
Report Source00
Date Received2015-01-16
Date of Report2014-12-16
Date of Event2011-01-05
Date Mfgr Received2014-12-16
Date Added to Maude2015-02-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA0
Event Location0
Manufacturer ContactEFFIE JEFFERSON
Manufacturer Street3015 CARRINGTON MILL BLVD.
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194332672
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetPARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRUSCH MALLONEY FR28F, P/N9213
Generic NameESOPHAGEL BOUGIE
Product CodeFAT
Date Received2015-01-16
Catalog NumberMEDICAL UNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC US


Patients

Patient NumberTreatmentOutcomeDate
10 2015-01-16

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