It was reported when using the unspecified bd abg syringe there was insufficient blood flow through the device.The following information was provided by the initial reporter.The customer stated: "when the patient underwent arterial blood collection, the arterial blood collection needle did not rise automatically, and the doctor felt that it had entered the artery, so the patient was not re-punctured.After withdrawing the needle plug, arterial blood was collected, without causing damage to the patient or causing material waste.".
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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.(b)(4).Medical device expiration date: unknown.Device manufacture date: unknown.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.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.
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