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.
[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
Report Number | 3004365956-2015-00016 |
MDR Report Key | 4432978 |
Report Source | 00 |
Date Received | 2015-01-16 |
Date of Report | 2014-12-16 |
Date of Event | 2011-01-05 |
Date Mfgr Received | 2014-12-16 |
Date Added to Maude | 2015-02-06 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 0 |
Initial Report to FDA | 0 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | EFFIE JEFFERSON |
Manufacturer Street | 3015 CARRINGTON MILL BLVD. |
Manufacturer City | MORRISVILLE NC 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer Phone | 9194332672 |
Manufacturer G1 | TELEFLEX MEDICAL |
Manufacturer Street | PARQUE INDUSTRIAL FINSA |
Manufacturer City | NUEVO LAREDO 88275 |
Manufacturer Country | MX |
Manufacturer Postal Code | 88275 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | RUSCH MALLONEY FR28F, P/N9213 |
Generic Name | ESOPHAGEL BOUGIE |
Product Code | FAT |
Date Received | 2015-01-16 |
Catalog Number | MEDICAL UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | RESEARCH TRIANGLE PARK NC US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-01-16 |