NASOGASTRIC SUMP TUBE DUAL LUMEN 0042180

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-10-14 for NASOGASTRIC SUMP TUBE DUAL LUMEN 0042180 manufactured by Productos Para El Cuidado De La Salud -9611590.

Event Text Entries

[57697524] The investigation is still in progress. Once the investigation is complete a supplemental report will be filed. The information provided by bard represents all of the known information at this time. Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bard. The device was not returned.
Patient Sequence No: 1, Text Type: N, H10


[57697605] It was reported that the nasogastric tube broke. The complainant alleged that the nasogastric tube was placed in the operating room and was hooked to low continuous wall suction. The patient pulled on the tube and as a result the tube broke while inside the nasal cavity. Half of the tube was pulled out of the nasal cavity. The complainant alleged that the ent was called and the tube was retrieved from the back of the patient's throat at the bedside. Another tube was inserted without incident. It was reported that no manipulation was done on the nasogastric tube prior to the break. No patient injury was reported.
Patient Sequence No: 1, Text Type: D, B5


[58627687] The investigation is still in progress. Once the investigation is complete a supplemental report will be filed. The device was not returned.
Patient Sequence No: 1, Text Type: N, H10


[58627688] It was reported that the nasogastric tube broke. The complainant stated that the nasogastric tube was placed in the operating room and was hooked to low continuous wall suction. The patient pulled on the tube and as a result the tube broke while inside of the nasal cavity. Half of the tube was pulled out of the nasal cavity. The complainant alleged that the ent was called and the tube was retrieved from the back of the patient's throat at the bedside. Another tube was inserted without incident. It was reported that no manipulation was done on the nasogastric tube prior to the break. No patient injury was reported.
Patient Sequence No: 1, Text Type: D, B5


[60912979] The device was not returned for evaluation. The lot number is unknown; therefore, the device history record could not be reviewed. The instructions for use states the following: "indications for use: bard nasogastric sump tubes are intended to be used for: decompression of stomach by suction or aspiration of gastric contents. Short-term administration of term tube feeding, lavage fluid and medications. Contraindications: patients with known tape or adhesive allergies. Warnings: use with caution in patients with a history of head trauma, facial trauma, esophageal diseases and patients with potential for vomiting. Do not force nasogastric tube during insertions; damage to the nasal passage and mucosa and bleeding may occur. Measure insertion length carefully- excessive insertion length of tube into the stomach may lead to coiling and/or formation of tube-knot. Lubricate the tube generously with water soluble lubricant prior to insertion. Do not use petroleum-based products as they may be harmful to the respiratory tract. Reflux of gastric contents into the blue vent lumen indicates that the suction lumen is obstructed or suction is too low. Routinely check for reflux in the blue vent lumen and clear as per applicable directions. Failure to clear the obstruction or clear prevent filter may cause gas & fluid buildup in stomach, aspiration of gastric contents, aspiration pneumonia and other complications. Do not inject fluid through the prevent filter as this may result in blockage and leakage of filter. Monitor patient for nasal erosion, sinusitis, esophagitis, esophagotracheal fistula, gastric erosion and pulmonary & oral infections. Statlock nasogastric stabilization device: avoid contact with alcohol or acetone; both can weaken bonding of components and statlock stabilization device pad adherence. Instructions for nasogastric tube insertion: explain the procedure to the patient. Carefully measure to find desired length of the tube using the nasogastric tube as a measurement aid. To determine the insertion length: measure the tube from the tip of the nose to the earlobe and from the earlobe to the tip of the xiphoid process. Mark the length of the tube to be passed with a small piece of tape. Check the patient? S nostrils for patency; select the nostril with best patency. Lubricate the full length of tube to be inserted. Insert the tube through the nose aiming down and back. When the tube hits the pharynx, if patient is able, have him or her flex his/her head forward and swallow. Advance the tube as the patient swallows. If resistance is met, rotating the tube may facilitate placement. Continue to advance the tube until the marked position on the tube is reached. Do not advance beyond the marked length as coiling and or knotting of the tube in the stomach may occur. Confirm tube placement per hospital policy. The tube has a radiopaque stripe facilitating x-ray confirmation. If proper placement of tube within the stomach cannot be confirmed, remove the tube gently and start the procedure again. Secure with a securement device or tape per hospital protocol. Ensure 5-in-1 adapter or lopez valve is snugly inserted into suction lumen to prevent suction loss. Keep blue vent lumen above the level of the patient? S stomach to prevent reflux of stomach fluids into the blue lumen. Do not clamp air vent port while suction is being applied. " (b)(4). The information provided by bard represents all of the known information at this time. Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bard.
Patient Sequence No: 1, Text Type: N, H10


[60912980] It was reported that the nasogastric tube broke. The complainant stated that the nasogastric tube was placed in the operating room and was hooked to low continuous wall suction. The patient pulled on the tube and as a result the tube broke while inside of the nasal cavity. Half of the tube was pulled out of the nasal cavity. The complainant alleged that the ent was called and the tube was retrieved from the back of the patient's throat at the bedside. Another tube was inserted without incident. It was reported that no manipulation was done on the nasogastric tube prior to the break. No patient injury was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2016-01404
MDR Report Key6030011
Date Received2016-10-14
Date of Report2016-10-28
Date of Event2016-08-24
Date Mfgr Received2016-10-28
Date Added to Maude2016-10-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJANNA PARKS
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal30014
Manufacturer Phone7707846100
Manufacturer G1PRODUCTOS PARA EL CUIDADO DE LA SALUD -9611590
Manufacturer StreetKM. 7 CARRETERA INTERNACIONAL
Manufacturer CityNOGALES, SONORA 85621
Manufacturer CountryMX
Manufacturer Postal Code85621
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNASOGASTRIC SUMP TUBE DUAL LUMEN
Generic NameNASOGASTRIC TUBE
Product CodeBSS
Date Received2016-10-14
Catalog Number0042180
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerPRODUCTOS PARA EL CUIDADO DE LA SALUD -9611590
Manufacturer AddressKM. 7 CARRETERA INTERNACIONAL NOGALES, SONORA 85621 MX 85621


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-10-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.