The customer's address is unknown.(b)(6) usa has been used as a default.Medical device expiration 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.Unknown manufacturer: (b)(4).
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It was reported that an unspecified bd posiflush syringe had a difficult to move plunger and a unit seal that was broken, compromising sterility.The following information was provided by the initial reporter: "material no: unknown batch no: unknown.It was reported via posiflush pmcf survey that the clinician experienced damaged packaging, plunger movement difficult, within the past 12 months while.See spreadsheet for full event details.".
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