FDA Adverse Event Malfunction Summary report: N

3002807968-2017-00049

MDR report key: 7141502 · Received December 22, 2017

Report

Report Number
3002807968-2017-00049
Event Type
Malfunction
Date Received
December 22, 2017
Date of Event
December 1, 2017
Report Date
October 3, 2018
PMA / PMN Number
K962158
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

ROOT CAUSE INVESTIGATION - THE ROOT CAUSE OF CORROSION IS EXPOSURE TO HIGH CONCENTRATIONS OF CHLORIDE CONTAINING GAS/LIQUID IN A HIGH TEMPERATURE & HIGH HUMIDITY ENVIRONMENT. - ANALYSIS AND INVESTIGATIONS HAVE BEEN MADE TO SUPPORT THIS ROOT CAUSE: CHLORIDE SALTS IDENTIFIED ON SYRINGES. FEO + FECL3 IDENTIFIED ON CORRODED NEEDLES. SIGNIFICANT SMELL OF CHLORIDE OF SAMPLERS WITH CORRODED NEEDLES. LITERATURE INVESTIGATION AND EXPERTS STATEMENTS. - BY TESTING OF REFERENCE SAMPLES, IT HAS BEEN CONCLUDED THAT EXPOSURE TO CHLORIDE OCCURS AFTER SAMPLERS HAVE BEEN SHIPPED TO (B)(4). - INVESTIGATION OF EACH STEP OF THE SUPPLY CHAIN HAS BEEN PERFORMED. - USE OF CHLORIDE CONTAINING GASES HAS NOT BEEN IDENTIFIED ANYWHERE IN THE SUPPLY CHAIN, AND WOULD NOT BE PRESENT DURING NORMAL HANDLING/STORAGE/SHIPPING. CONCLUSION IS THAT NO SYSTEMATIC PATTERN OF NEEDLE CORROSION CAN BE FOUND. THE CORROSION IS LIMITED TO A FEW NEEDLES OF EACH LOT, AND WILL NOT BE PRESENT DURING INTENDED HANDLING, STORAGE AND SHIPPING.

Description of Event or Problem · 1

ACCORDING TO THE COMPLAINT, THE SURFACE OF THE NEEDLE ON A PICO70 SAMPLER IS REPORTED AS BEING RUSTY. NONE OF THE PICO70 SAMPLERS WITH RUST ON HAS BEEN USED ON PATIENTS, ALL PICO70 ARE STILL IN SEALED PACKAGING.

Patients

Seq Age Sex Outcome Treatment
1