MAUDE Adverse Event Report: AVANOS MEDICAL INC. NEOMED PVC FEEDING TUBES (ENFIT); DH NASOGASTRIC (NG) FEEDING TUBES (NEOMED AND NEOCONNECT)

Model Number PFTM6.5V-NC

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Apnea (1720); Hemorrhage/Bleeding (1888); Hyperbilirubinemia (1903); Respiratory Distress Syndrome of Newborns (2046); Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)

Event Type  Injury  

Manufacturer Narrative

The actual complaint product was not returned for evaluation.A review of the device history record is in-progress.All information reasonably known as of 17 jan 2023 has been included in this health authority report.Should additional information be obtained, a follow-up health authority report will be provided.The information provided by avanos medical inc.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 avanos medical inc.Avanos medical inc.Has no independent knowledge of the event reported but is relaying the information that was provided by the user facility where the incident occurred.This product incident is documented in the avanos medical complaint database and identified as complaint (b)(4).This information is submitted pursuant to 21cfr803, in compliance with the medical device reporting requirement and should not be considered to be an admission that an avanos medical inc.Product is defective or caused serious injury.Device not returned.

Event Description

Avanos medical inc.Received a single report that referenced two different incidences, which were associated with separate units, involving two different patients.This is the second of two reports.Refer to 3011270181-2023-00003 for the first report.It was reported, the infant had gastrointestinal (gi) bleeding for which no clear cause was established.No medical intervention was reported.The infant¿s current condition was not reported.

Event Description

Additional information received 27jan2023 reported, the preterm infant was delivered by cesarean section due to hellp syndrome (hemolysis with a microangiopathic blood smear, elevated liver enzymes, and a low platelet count).Apgar scores 9 and 9 and 1 and 5 minutes, respectively.An orogastric tube was placed on admission, it was later changed to a nasogastric tube; initial feedings consisted of breast milk and later breast milk fortified with liquid human milk.Selected diagnoses and treatments in nicu: respiratory distress syndrome treated with supplemental o2 and continuous positive airway pressure.Apnea of prematurity not requiring caffeine.Hyperbilirubinemia requiring monitoring but not phototherapy.Bloody stools.On day of life (dol) 6, the infant had a small amount of blood in the stool with otherwise normal exam.Exam, radiographs and laboratory studies were normal, liquid human milk fortifiers (hmf) removed from feedings.On dol 11, the infant had greatly increased amounts of blood in the stool repeat kidney urethra and bladder (kub) exams were equivocal, feedings were stopped, and the infant received antibiotics for 7 days which were subsequently successfully; the infant was refed with an elemental formula and did well.The final diagnosis believed to be allergic colitis.

Manufacturer Narrative

H6: appropriate clinical signs, symptoms, conditions term/code not available: bloody stools.H6: (appropriate health impact term/code not available): supplemental o2 and continuous positive airway pressure.The device history record for lot ty220825 was reviewed and the product was produced according to product specifications.All information reasonably known as of 16 feb 2023 has been included in this health authority report.Should additional information be obtained, a follow-up health authority report will be provided.The information provided by avanos medical inc.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 avanos medical inc.Avanos medical inc.Has no independent knowledge of the event reported but is relaying the information that was provided by the user facility where the incident occurred.This product incident is documented in the avanos medical complaint database and identified as complaint (b)(4).This information is submitted pursuant to 21cfr803, in compliance with the medical device reporting requirement and should not be considered to be an admission that an avanos medical inc.Product is defective or caused serious injury.

• Brand Name: NEOMED PVC FEEDING TUBES (ENFIT)
• Type of Device: DH NASOGASTRIC (NG) FEEDING TUBES (NEOMED AND NEOCONNECT)
• Manufacturer (Section D): AVANOS MEDICAL INC.; 5405 windward parkway; alpharetta GA 30004
• Manufacturer (Section G): NINGBO TIANYI MEDICAL APPLIANCE CO., LTD; no.788,mozhi north rd; tourism resort; dongqian lake, ningbo zhejiang
• Manufacturer Contact: lisa clark ; 5405 windward parkway; alpharetta, GA 30004 ; 4704485444
• MDR Report Key: 16187636
• MDR Text Key: 307520481
• Report Number: 3011270181-2023-00004
• Device Sequence Number: 1
• Product Code: KNT
• UDI-Device Identifier: 00350770001876
• UDI-Public: 00350770001876
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K120182
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,User Facility,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 02/17/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/17/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: PFTM6.5V-NC
• Device Lot Number: TY220825
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 01/27/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 08/26/2022
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Outcome(s): Other