Device Problem
Contamination (1120)
|
Patient Problem
Urinary Tract Infection (2120)
|
Event Type
Injury
|
Manufacturer Narrative
|
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.
|
|
Event Description
|
It was reported that the patient experienced a urinary tract infection while using the catheter.
|
|
Manufacturer Narrative
|
The device was not returned for evaluation.The lot number is unknown; therefore, the device history record could not be reviewed.The product family for this silicone catheter product is unknown.Therefore, bard is unable to determine the associated labeling to review.Although the product family is unknown, the silicone catheter product ifus are found to be adequate based on past reviews.(b)(4) the device was not returned.
|
|
Event Description
|
It was reported that the patient experienced a urinary tract infection while using the catheter.
|
|
Search Alerts/Recalls
|