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Patient 1
THE DISTRIBUTOR REPORTED THE SHIPMENT CONTAINING STOP SOLUTION (1N SODIUM HYDROXIDE) WAS RECEIVED WITH A STAINED CARTON, SUGGESTING LEAKAGE OF AN ITEM IN THE PACKAGE. PHOTOGRAPHIC EVIDENCE PROVIDED BY THE DISTRIBUTOR SHOWED TWO STAINED CARTONS. PICTURES OF THE STOP SOLUTION BOTTLES SHOWED THAT ONE BOTTLE HAD A VISIBLY LOWER VOLUME THAN THE BOTTLE FROM THE OTHER CARTON. HYCOR REQUESTED PRODUCTS BE RETURNED FOR INVESTIGATION. THE INVESTIGATION DEMONSTRATED ONE OF THE TWO RETURNED BOTTLES WAS LEAKING AS DETERMINED BY A VACUUM TEST. FURTHER INVESTIGATION DETERMINED THAT THE STOP SOLUTION BOTTLES USED IN THE KIT LOT WERE MANUFACTURED DURING A TIME WHEN THE AUTOMATIC CAPPING SYSTEM MALFUNCTIONED LEADING TO A TEMPORARY PROCESS TO HAND TIGHTEN THE CAPS. A STOP SHIP ORDER FOR PRODUCT CONTAINING STOP SOLUTION BOTTLES MANUFACTURED DURING THE TIME PERIOD WHEN THE CAPPING SYSTEM WAS NOT FUNCTIONING CORRECTLY WAS INITIATED 05/31/2018. ALL IMPACTED BOTTLES OF STOP SOLUTION HAVE BEEN REPROCESSED ENSURING THAT THE CAP IS SEALED WITH THE PROPER TORQUE. A SAMPLING OF PRODUCT WAS TESTED IN A VACUUM CHAMBER TO DETERMINE IF LEAKING WAS PRESENT, NO LEAKS WERE DETECTED. HYCOR IS INITIATING A RECALL ACTION TO INFORM DISTRIBUTORS THAT LEAKING STOP SOLUTION BOTTLES HAVE BEEN REPORTED DURING TRANSIT AND THAT THEY SHOULD INSPECT REMAINING INVENTORY FOR EVIDENCE OF LEAKAGE PRIOR TO FURTHER DISTRIBUTION. THERE WERE NO ADVERSE OUTCOMES REPORTED TO HYCOR. HOWEVER, OUT OF AN ABUNDANCE OF CAUTION, WE ARE FILING AN MDR. DELAY IN REPORTING WAS DUE TO AN EMPLOYEE CONFUSING THIS EVENT WITH A PREVIOUSLY REPORTED SIMILAR EVENT, REVIEW OF RECORDS DETERMINED THAT THIS EVENT SHOULD ALSO HAVE BEEN REPORTED. [(B)(4)].