Reference record (b)(4).The device manufacturer and lot number of the device involved in this complaint was not provided.Therefore, it is unknown if the device involved was abbvie branded tubing.Conservatively, abbvie has chosen to report this complaint due to the potential that the device involved could have been abbvie branded tubing.It was unknown if the device involved in the event was discarded or will be returned; therefore, a return sample evaluation is unable to be performed.However, if the device is received, a follow up report will be submitted upon completion of the return sample investigation.A duodenal ulcer is a known complication of a j tube placement.If any further relevant information is identified or obtained, a supplemental medwatch will be filed.
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On an unknown date, a patient in japan underwent a procedure for the placement of percutaneous endoscopic jejunal tube (j-tube).On (b)(6) 2020, the patient experienced an ulcer in the duodenum.On (b)(6) 2020, the ulcer in the duodenum resolved.It was unknown if the patient received any treatment or medical interventions.No further information was available.
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