Date of event: unknown.The date received by manufacturer has been used.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.Medical device expiration date: unknown.Device manufacture date: unknown.(b)(4).Investigation summary: bd was unable to perform a thorough investigation as no sample, lot, or batch number were provided.Complaints received for this device and reported condition will continue to be tracked and trended.Information will be captured on trend reports and monitored monthly.Our business team regularly reviews the collected data for identification of emerging trends.Per bd corrective and preventive action (capa) corporate procedure, the reported issue does not represent a single significant incident that would trigger a capa.
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It was reported that unspecified bd¿ connecta had flow issues, leakage, disconnected stopcock, tubing kinked, damaged device, and open package seal.The following information was provided by the initial reporter: material no: unknown, batch no: unknown.It was reported via post market survey that the clinician encountered occurrences of infection (blood stream bacteraemia, sepsis etc.) (8), no flow or reduced flow of fluids (4), leakage (6), stopcock inadvertently disconnects from mating component (14), tubing kinked (25), the bd connecta¿ stopcock is defective or damaged (2), and the package seal open before use (8).
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