Reference record (b)(4).The device involved in the event remained implanted in the patient and was not returned; therefore, a return sample evaluation is unable to be performed.Catalog number in d4 is the similar us list number, the international list number is unknown.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.Aspiration pneumonia is a known complication of a peg tube/ j-tube placement.If any further relevant information is identified or obtained, a supplemental medwatch will be filed.
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On (b)(6) 2024, a patient in germany underwent a procedure for the replacement of the jejunal (j) tube.On 05 jan 2024, the patient was hospitalized due to pneumonia.On (b)(6) 2024, the patient was discharged from the hospital.No further information was provided.
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