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Catalog Number DYNDTN1603 |
Device Problems
Crack (1135); Improper Flow or Infusion (2954)
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Patient Problem
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
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Event Date 07/01/2022 |
Event Type
Injury
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Manufacturer Narrative
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It was reported that during a procedure the iv tubing line cracked at the connection port resulting in the patient not receiving the required medication to effectively keep them asleep.Per the facility new tubing was required and the medication line was changed.According to the facility the patient required anesthesia intervention, however, the patient's recovery was not impacted.Photos have been returned that show the customer reported issue to be confirmed however a definitive root cause has not been established.No additional information is available at this time.Due to the reported incident and in an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.
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Event Description
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It was reported that, during a procedure the iv tubing line cracked at the connection port causing the patient to not receive the required medication to effectively keep them asleep.According to the facility the patient required anesthesia intervention.
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Search Alerts/Recalls
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