It was reported that the tip of the feeding syringe was different and did not feet into a feeding tube.No serious injury or adverse impact to a patient or user was originally reported.To date, no information has been received to indicate that a user or a patient experienced a death, serious injury, medical intervention, follow-up care, or other adverse health impact associated with the reported problem/issue.A sample was returned for evaluation.The reported problem/issue was not confirmed as a device defect.An abundance of caution, and in response to an fda 483 issued for (b)(4) on (b)(6)2024, this medwatch is being filed.If additional relevant information becomes available a supplemental medwatch will be filed.
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