Catalog Number UNKNOWN |
Device Problem
Failure to Deliver (2338)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/08/2022 |
Event Type
malfunction
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Manufacturer Narrative
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A device evaluation is anticipated but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.Device expiration date: unknown, device manufacture date: unknown.Unknown manufacturer: there are multiple bd locations where this unspecified bd device may have been manufactured.A catalog and lot number could not be confirmed for this incident and without this information we are unable to determine where the device was manufactured.Therefore, bd corporate headquarters in (b)(4) has been listed and the (b)(4) fda registration number has been used for the manufacture report number.
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Event Description
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It was reported that the unspecified bd pen needle did not deliver the insulin.The following information was provided by the initial reporter, translated from german to english: insulin is not delivered; mr.(b)(6) has to change up to three times until insulin is delivered.
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Event Description
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It was reported that the unspecified bd pen needle did not deliver the insulin.The following information was provided by the initial reporter, translated from german to english: insulin is not delivered; mr.X has to change up to three times until insulin is delivered.
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Manufacturer Narrative
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H6: investigation summary: no samples (including photos) were returned therefore the complaint could not be confirmed and the root cause is undetermined.No dhr review can be carried out as lot number is unknown.
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Search Alerts/Recalls
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