It was reported when using the bd posiflush¿ normal saline syringe the plunger had difficult movement.The following information was provided by the initial reporter.The customer stated: "when the nurse prepared to flush the tube for port patient and connected the needle-free infusion connector, the flush¿s plunger could not move, so it was discarded and replaced.".
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Medical device expiration date: unknown.Device manufacture date: unknown.Investigation summary: as no physical sample, picture sample, or lot number was provided for evaluation by our quality engineer team, a complete investigation could not be performed.There are current quality controls in place to detect this type of product malfunction during the production process.Based on the limited investigation results, a cause for the reported incident could not be determined.Examination of the product involved may provide clarification as to the cause for the reported failure.
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