There was/were 3 case(s) with a sample received for evaluation, a result code of no findings available and a conclusion code of cause not established.There was/were 23 case(s) with no sample received for evaluation, a result code of no findings available and a conclusion code of cause not established.There was/were 3 case(s) with a sample received for evaluation, a result code of operational problem identified and a conclusion code of cause not established.There was/were 6 case(s) with a sample received for evaluation, a result code of operational problem identified and a conclusion code of cause cannot be traced to device.There was/were 1 case(s) with no sample received for evaluation, a result code of improper material and a conclusion code of failure to follow instructions.There was/were 1 case(s) with a sample received for evaluation, a result code of no findings available and a conclusion code of failure to follow instructions.There was/were 1 case(s) with no sample received for evaluation, a result code of no findings available and a conclusion code of failure to follow instructions.There was/were 1 case(s) with a sample received for evaluation, a result code of operational problem identified and a conclusion code of failure to follow instructions.There was/were 2 case(s) with no sample received for evaluation, a result code of operational problem identified and a conclusion code of failure to follow instructions.There was/were 1 case(s) with no sample received for evaluation, a result code of operational problem identified and a conclusion code of cause cannot be traced to device.The manufacturer internal reference number is: 2019-53473.
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This report summarizes 39 events for q2 2019.There was/were 15 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code defective device.There was/were 1 female, (b)(6), unknown weight patient(s) with reported event(s) of device code defective device.There was/were 1 male, (b)(6), unknown weight patient(s) with reported event(s) of device code defective device.There was/were 2 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code device contamination with chemical or other material.There was/were 1 male, (b)(6), unknown weight patient(s) with reported event(s) of device code scratched material.There was/were 1 female, (b)(6), unknown weight patient(s) with reported event(s) of device code scratched material.There was/were 8 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code scratched material.There was/were 3 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code crack.There was/were 2 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code material split, cut or torn.There was/were 1 male, (b)(6), unknown weight patient(s) with reported event(s) of device code inaccurate delivery.There was/were 1 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code break.There was/were 1 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code material opacification.There was/were 1 unknown gender, unknown age, unknown weight patient(s) with reported event(s) of device code material twisted / bent.There was/were 1 male, (b)(6), unknown weight patient(s) with reported event(s) of device code failure to advance.
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