Catalog Number 367986 |
Device Problem
Improper or Incorrect Procedure or Method (2017)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 11/09/2023 |
Event Type
malfunction
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Manufacturer Narrative
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H.3.A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.D.4.Medical device expiration date: unknown.H.4.Device manufacture date: unknown.
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Event Description
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It was reported when using the bd vacutainer® sst¿ blood collection tubes customer used the tube one week past expiration.There was no report of impact to patient or user.
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Event Description
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It was reported when using the bd vacutainer® sst¿ blood collection tubes customer used the tube one week past expiration.There was no report of impact to patient or user.
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Manufacturer Narrative
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H6: investigation summary: bd had not received samples or photos for evaluation.Additionally, bd was unable to determine the specific lot number associated with this complaint; therefore, a review of the device history record could not be conducted.Bd makes no claims on expired product.This complaint is unable to be confirmed.If additional information is made available, this complaint will be reopened to assess the level of investigation needed.Complaints received for this device and reported condition will continue to be tracked and trended.Our business team regularly reviews the collected data for identification of emerging trends.
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Search Alerts/Recalls
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