Catalog Number UNKNOWN |
Device Problem
Loose or Intermittent Connection (1371)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 06/28/2023 |
Event Type
malfunction
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Manufacturer Narrative
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B.3.Date of event: unknown.The date received by manufacturer has been used for this field.D.4 device expiration date: unknown.H3.A device evaluation is anticipated but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.H.4.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 franklin lakes, nj has been listed in sections d.3.And g.1.And the franklin lakes 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¿ syringe plunger falls out.The following information was provided by the initial reporter: the plunger pulling out.
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Event Description
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It was reported that the unspecified bd¿ syringe plunger falls out.The following information was provided by the initial reporter: the plunger pulling out.
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Manufacturer Narrative
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H6: investigation summary as no physical sample, valid part number or lot number was provided for evaluation by our quality engineer team, a complete investigation could not be performed.Material or plant could not be determined from the provided images.Based on the limited investigation results, a cause for the reported incident could not be determined.See h.10.
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Search Alerts/Recalls
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