C.R. BARD, INC. (BASD) -3006260740 POWERLOC SAFETY INFUSION SET 20G X 0.75IN; SET, ADMINISTRATION, INTRAVASCULAR
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Model Number N/A |
Device Problem
Material Twisted/Bent (2981)
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Patient Problem
Pain (1994)
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Event Date 02/29/2024 |
Event Type
malfunction
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Manufacturer Narrative
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H11: section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.The manufacturer has received the sample and will evaluate.Results are expected soon.
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Event Description
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It was reported, ¿a 3/4-inch needle bent when accessing a patient.The rn accessed the patient's implanted port per usual protocol, and entered in the middle of the port.Although the needle was in the middle of the port, however, it did not flush.When the rn removed the hubert needle, she noted that the needle was bent.The patient expressed that the access was more painful than usual, and he complained that it felt sore after, which is not typical.¿ no other information was provided.
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Manufacturer Narrative
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H11: the initial complaint appeared to be a reportable occurrence.Once the sample was returned and evaluated it was determined that a reportable event had not occurred.H3 other text : evaluation findings are in section h11.
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Event Description
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It was reported, ¿a 3/4-inch needle bent when accessing a patient.The rn accessed the patient's implanted port per usual protocol, and entered in the middle of the port.Although the needle was in the middle of the port, however, it did not flush.When the rn removed the hubert needle, she noted that the needle was bent.The patient expressed that the access was more painful than usual, and he complained that it felt sore after, which is not typical.¿ no other information was provided.
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