BARD INLAY URETERAL STENT
Report
- Report Number
- 1018233-2022-00574
- Event Type
- Malfunction
- Date Received
- February 12, 2022
- Date of Event
- January 19, 2022
- Report Date
- April 26, 2022
- Manufacturer
- C.R. BARD, INC. (COVINGTON) -1018233
- Product Code
- FAD
- PMA / PMN Number
- K983498
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE A SUPPLEMENTAL REPORT WILL BE FILED.
THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE A SUPPLEMENTAL REPORT WILL BE FILED.
THE REPORTED EVENT WAS CONFIRMED TO BE A DESIGN ISSUE. RECEIVED ONLY PHOTO. BASED ON PHOTO ATTACHED, OBSERVATIONS FOUND THAT THERE WAS ERROR ON THE LABELLING OF INNER CARTON LABEL VERSUS POUCH PRINTED LABEL. BASED ON THE INFORMATION PRINTED ON INNER CARTON LABEL (PL8109), IT WAS STATED THAT THIS PRODUCT IS PRINTED WITH REIMBURSEMENT CODE ¿I¿ AND CONTRADICT WITH THE LABEL PRINTED ON THE POUCH LABEL (PL8078). THEREFORE, THE REPORTED EVENT OF INCORRECT CODE FOR PRODUCT 874626 IS CONFIRMED. BASED ON THE HISTORICAL CHANGES ON LABEL ARTWORK, ACCORDING TO THE MHLW REQUIREMENT, THIS PRODUCT IS IMPLEMENTED WHEREBY THERE ARE COMMONLY CHANGED REIMBURSEMENT CODE FROM CATEGORY II TO CATEGORY I ON (B)(6) 2018. THIS CHANGE IS ONLY AFFECTED TO THE INNER CARTON LABEL AND NOT UPDATED FOR INLAY STENT POUCH LABEL. THE DEVICE HISTORY RECORD WAS REVIEWED AND FOUND NOTHING THAT COULD HAVE CAUSED OR CONTRIBUTED TO THE REPORTED EVENT. THE INSTRUCTIONS FOR USE WERE FOUND ADEQUATE AND STATE THE FOLLOWING: ¿[WARNINGS] 1. METHOD FOR USE (1) WHEN USING THE MULTI-LENGTH TYPE, USE SHOULD BE AVOIDED IN THE FOLLOWING CASES. 1) MEASURE THE LENGTH OF PATIENT¿S URETER AND CONFIRM THAT EXCESSIVE COIL PARTS WILL NOT BE FORMED. CONSIDER USE OF OTHER STENT LENGTHS DEPENDING ON RISK. URETERAL STENTS WITH EXCESSIVE COIL PARTS HAVE RISKS OF KNOT FORMATION AT THE TIP OF THE RENAL PELVIS SIDE DURING PLACEMENT OR REMOVAL. 1) 2) IF ANY RESISTANCE IS FELT DURING REMOVAL, CONFIRM THE CAUSE OF THE RESISTANCE UNDER FLUOROSCOPY AND TAKE REMEDIAL ACTION TO SOLVE THE PROBLEM. EXCESSIVE FORCE DURING REMOVAL MAY LEAD TO DAMAGE OF THE RENAL PELVIS AND/OR URETER. (2) URETEROARTERIAL FISTULA MAY BE FORMED BETWEEN THE URETER AND THE AORTA OR THE ILIAC ARTERY AND RESULT IN MASSIVE HEMORRHAGE AT THE REPLACEMENT OF THE URETERAL STENT IF A URETERAL STENT IS PLACED FOR A LONG TERM IN A PATIENT WHO HAS UNDERGONE THE INTRAPELVIC SURGERY OR IRRADIATION. THEREFORE, CAREFULLY MONITOR THE CONDITION OF THE PATIENT, AND IN THE EVENT OF ACKNOWLEDGING BLEEDING FROM THE URETHRA, PERFORM RETROGRADE PYELOGRAPHY OR ANGIOGRAPHY, AND PROVIDE APPROPRIATE CARE. [CONTRAINDICATIONS] 1. METHOD FOR USE (1) DO NOT REUSE. (2) DO NOT RESTERILIZED. 2. APPLICABLE PATIENTS DO NOT USE FOR THE WOMAN WHO IS PREGNANT OR MAY BECOME PREGNANT. [TO AVOID RADIATION EXPOSURE ON PRE-BORN BABY FROM X-RAY.] [SHAPE, CONFIGURATION AND PRINCIPLES] BARD INLAY® STENT TRI-PAK® COMPRISES THE FOLLOWING COMPONENTS. 1. INLAY® URETERAL STENT THE INLAY URETERAL STENT IS A DOUBLE PIGTAIL URETERAL STENT WITH MONOFILAMENT SUTURE LOOP ATTACHED TO AID IN STENT REMOVAL. THE STENT IS AVAILABLE IN TWO FORMS: A SINGLE SIZE OR A CUSTOMIZED MULTI-LENGTH SIZE. SOME OF THE SINGLE SIZE TYPE HAVE NO SIDE HOLE. <MATERIAL> POLYURETHANE. 2. PUSHER WITH RADIOPAQUE TIP <MATERIAL> POLYETHYLENE 3. TIGER TAIL URETERAL CATHETER <MATERIAL> POLYURETHANE BARD SOLO GUIDEWIRE <MATERIAL> POLYURETHANE, STAINLESS STEEL, POLYTETRAFLUOROETHYLENE, EPOXY, SILANE COUPLING AGENT, POLYVINYLPYRROLIDONE, NI-TI-CO ALLOY. [INTENDED USE & EFFECT- EFFICACY] BARD INLAY® TRI-PAK® TRAY WITH BARD SOLO GUIDEWIRE IS A SET OF MEDICAL DEVICES. IT CONSISTS OF A DISPOSABLE STENT TO BE INSERTED INTO THE URETER AND USED FOR THE DRAINAGE OF URINE IN ORDER TO SECURE A URINARY PASSAGE FROM THE PYELOTRANSITIONAL AREA TO THE BLADDER, DISPOSABLE URETERAL CATHETER CAN TEMPORARILY INDWELL IN THE RENAL PELVIS OR THE URETER IN ORDER TO PERFORM PYELOGRAPHY AND FOR DILATION OF URETERAL STRICTURE, AND GUIDEWIRE CAN BE USED FOR INSERTION OF THE STENT. [DIRECTIONS FOR USE] 1. METHOD OF USE DETERMINE THE PROPER STENT LENGTH FOR THE PATIENT. THIS IS GENERALLY CALCULATED FROM THE BASELINE PYELOGRAM. ACCURATE MEASUREMENTS WILL OPTIMIZE DRAINAGE EFFICIENCY AND PATIENT COMFORT. (1) INSERTION OF THE GUIDEWIRE 1) INJECT PHYSIOLOGICAL SALINE SOLUTION INTO THE LUER OF THE PROTECTIVE HOOP IN ORDER TO COMPLETELY WET THE SURFACE OF THE GUIDEWIRE. 2) REMOVE THE GUIDEWIRE FROM THE PROTECTIVE HOOP. 3) INSERT THE GUIDEWIRE EITHER THROUGH THE WORKING CHANNEL OF AN ENDOSCOPE OR PERCUTANEOUSLY, WITH THE SOFT END OF THE GUIDEWIRE FIRST. 4) ADVANCE THE GUIDEWIRE INTO THE DESIRED POSITION UNTIL THE TIP IS IN THE RENAL PELVIS. CONTINUOUSLY CONFIRM GUIDEWIRE POSITION EITHER VISUALLY OR UNDER FLUOROSCOPY. (2) NEPHROURETEROGRAPHY 1) PLACE THE URETERAL CATHETER OVER THE GUIDEWIRE AND INSERT IT INTO THE URETER. IN THIS CASE, IT IS ALSO POSSIBLE INSERT THE URETERAL CATHETER WITHOUT USING A GUIDEWIRE, AT THE DISCRETION OF A PHYSICIAN. 2) CAREFULLY AND SLOWLY WITHDRAW THE GUIDEWIRE FROM THE PATIENT TO AVOID ANY KINKING. 3) ATTACH THE URETERAL CATHETER ADAPTER TO THE TIP OF THE URETERAL CATHETER FOR PERFORMING DRAINAGE OF URINE, RETROGRADE VISUALIZATIONS, AND SO ON. 4) INTRODUCE THE GUIDEWIRE AGAIN FOR STENT PLACEMENT AND REMOVE THE URETERAL CATHETER FROM THE CYSTOSCOPE. (3) STENT PLACEMENT 1) IN ORDER TO IMPROVE SLIDING, IMMERSE THE STENT IN A NORMAL SALINE SOLUTION. 2) CONFIRM THE GUIDEWIRE POSITION WHERE IT COILS INSIDE THE RENAL PELVIS. 3) MOVE THE PIGTAIL STRAIGHTENER OVER THE PROXIMAL END (KIDNEY COIL END WITHOUT THE SUTURE) OF THE URETERAL STENT ALLOWING EASIER INSERTION ONTO THE GUIDEWIRE. 4) REMOVE PIGTAIL STRAIGHTENER ONCE THE STENT IS SECURE ON THE GUIDEWIRE. 5) KEEP WATCHING THE DISTAL END (BLADDER COIL END WITH THE SUTURE) OF THE STENT OR RADIOPAQUE, PROXIMAL END OF THE PUSHER WHILE ADVANCING TO PROPER POSITION OF THE STENT. HOLD THE GUIDEWIRE TO KEEP IT FROM MOVING. 6) STOP ADVANCING WHEN THE STENT¿S DISTAL END (BLADDER COIL END WITH THE SUTURE) IS WATCHED. IF THE PROXIMAL END IS INSERTED TOO MUCH, PULL THE SUTURE TO MODIFY THE STENT PROPERLY. 7) CONFIRM PROXIMAL END OF THE PUSHER AND STENT¿S DISTAL END MARKER (BLADDER END), REACHES THE URETEROVESICAL JUNCTION (UVJ) BY THE RADIOPAQUE. 8) HOLDING THE STENT IN POSITION WITH THE PUSHER, CUT THE SUTURE AND PULL IT OUT. 9) CAREFULLY AND SLOWLY WITHDRAW THE GUIDEWIRE FROM THE PATIENT TO AVOID ANY KINKING AND REMOVE THE PUSHER. THE STENT WILL FORM A PIGTAIL AUTOMATICALLY. 10) THE POSITION FOR PLACING THE STENT SHOULD BE CHECKED BY RADIOSCOPY. <MULTI-LENGTH URETERAL STENT> THE FIRST (WIDE) MARKER BAND ON THIS DEVICE INDICATES 22 CM, FOLLOWED BY TWO NARROW BANDS AT 24 CM AND 26 CM. THE LAST (WIDE) ONE INDICATES 28 CM. IF YOU NEED TO PLACE THE 30 CM OR 32 CM LENGTHS, USE THE ATTACHED SUTURE OR ENDOSCOPIC FORCEPS TO GENTLY PULL BACK ON THE STENT, UNWINDING THE COIL FROM THE KIDNEY. 2. PRECAUTIONS FOR USE <URETERAL CATHETER> (1) WHEN USING THE TIGER TAIL URETERAL CATHETER, ESPECIALLY WITHOUT THE STABILIZING. SUPPORT OF A GUIDEWIRE, BE AWARE THAT A MALFUNCTION MAY OCCUR WHERE THE FLEXIBLE TIP MAY DETACH IF EXCESSIVE FORCE IS MADE IN CONTACT WITH THE WALLS OF THE BLADDER, URETER OR RENAL PELVIS. SHOULD THE FLEXIBLE TIP PORTION OF THE CATHETER BECOME DETACHED, RETRIEVE WITH AN ENDOUROLOGY GRASPING DEVICE. (2) DO NOT WITHDRAW THE URETERAL CATHETER WHILE IT IS DEFLECTED IN ENDOSCOPE. (3) AVOID SHARP BENDING. (4) WHEN PERFORMING DRAINAGE OF URINE, RETROGRADE VISUALIZATIONS ETC. THOUGH THE URETERAL CATHETER, ATTACH THE URETERAL CATHETER ADAPTER TO THE TIP OF URETERAL CATHETER. (5) DO NOT OVER-TIGHTEN THE CATHETER ADAPTER. OVER-TIGHTENING OF THE CATHETER ADAPTER MAY OCCLUDE THE LUMEN OF THE CATHETER. <STENT> (1) DO NOT FORCIBLY INSERT OR REMOVE THE STENT. IT MAY INJURE THE SURROUNDING TISSUE OR DAMAGE THIS PRODUCT. (2) AVOID IMPROPER HANDLING WHICH MAY AFFECT THE INTEGRITY OF THIS DEVICE, INCLUDING BENDING, KINKING, OR TEARING. (3) EXERCISE CAUTION TO AVOID DAMAGING THE STENT WITH SHARP INSTRUMENTS. THIS MAY CAUSE THIS DEVICE TO TEAR, BREAK, OR FRAGMENT. (4) DETERMINE THE PROPER STENT LENGTH FOR THE PATIENT. SELECTION OF TOO SHORT A STENT MAY RESULT IN MIGRATION. (5) THE SUTURE ATTACHED TO THE STENT MAY BE CUT OFF PRIOR TO OR AFTER PLACEMENT. REMOVE THE SUTURE BEFORE PLACING THE STENT IN CHILDREN. REMOVE THE SUTURE IF INDWELLING TIME IS EXPECTED TO BE LONGER THAN 14 DAYS. (6) IN THE EVENT OF STENT MIGRATION, CYSTOSCOPY OR URETEROSCOPY SHOULD BE USED TO RETURN THE STENT TO THE ORIGINAL POSITION OR REMOVE FROM THE PATIENT BODY. (7) ANY SIGNS OF INFECTION IN THE LOCATION OF THE STENT PLACEMENT REQUIRE REMOVAL OF THE STENT. AFTER CHECKING THE CONDITION OF THE PATIENT, A NEW STENT SHOULD BE PLACED. (8) CARE SHOULD BE EXERCISED WHEN REMOVING THE STENT TO ELIMINATE TEARING OR FRAGMENTATION. <GUIDEWIRE> (1) WHEN WETTING THE SURFACE OF THE GUIDEWIRE, USE OF ALCOHOL, ANTISEPTIC SOLUTION OR OTHER SOLVENTS MUST BE AVOIDED [ALCOHOL, ANTISEPTIC SOLUTION OR OTHER SOLVENTS MAY ADVERSELY AFFECT THE SURFACE OF THE GUIDEWIRE.] (2) SAVE THE HOOP TO STORE THE GUIDEWIRE IF IT WILL BE USED AGAIN DURING THE SAME PROCEDURE ON THE SAME PATIENT. WHEN REINSERTING THE GUIDEWIRE BACK INTO THE HOLDER, TAKE CARE NOT TO DAMAGE THE WIRE¿S COATING WITH THE EDGE OF THE HOLDER. (3) DO NOT WIPE THE GUIDEWIRE WITH DRY GAUZE ETC. (4) KEEP AT LEAST 5 CM OF THE WIRE EXTENDED OUT OF THE PROXIMAL END OF THE SCOPE OR CATHETER DURING INTRODUCTION AT ALL TIMES. (5) BEFORE INSERTING THE GUIDEWIRE THROUGH A CATHETER, FILL THE CATHETER WITH PHYSIOLOGICAL SALINE SOLUTION. (6) THE GUIDEWIRE SHOULD BE ADVANCED THROUGH THE SCOPE USING SHORT, DELIBERATE 2-3 CM MOVEMENTS TO PREVENT INADVERTENT DAMAGE TO THE DEVICE OR PATIENT. (7) IF ANY RESISTANCE IS FELT DURING INTRODUCTION OF THE CATHETER, IT IS ADVISABLE TO STOP USING SUCH CATHETERS. [DUE TO VARIATIONS OF CERTAIN CATHETER TIP INNER DIAMETERS, ABRASION OF THE HYDROPHILIC COATING MAY OCCUR DURING MANIPULATION.] (8) AFTER REMOVAL FROM THE PATIENT¿S URINARY SYSTEM, AND PRIOR TO REINSERTING IT INTO THE SAME PATIENT DURING THE SAME CATHETERIZATION, HYDROPHILIC TIPPED GUIDEWIRES SHOULD BE RINSED IN A BOWL FULL OF PHYSIOLOGICAL SALINE SOLUTION. USE OF ALCOHOL, ANTISEPTIC SOLUTIONS OR OTHER SOLVENTS MUST BE AVOIDED. [USE OF ALCOHOL, ANTISEPTIC SOLUTIONS OR OTHER SOLVENTS MAY ADVERSELY AFFECT THE SURFACE OF THE GUIDEWIRE.] [PRECAUTIONS] 1. IMPORTANT PRECAUTIONS <STENT> (1) THE STENT IS NOT INTENDED AS A PERMANENT INDWELLING DEVICE. IT IS RECOMMENDED THAT THE INDWELLING TIME NOT EXCEED 365 DAYS. PERIODIC CHECKS OF THE STENT BY CYSTOSCOPIC AND/OR RADIOGRAPHIC PROCEDURES ARE RECOMMENDED AT INTERVALS DEEMED TO BE APPROPRIATE BY THE PHYSICIAN IN CONSIDERATION OF THE INDIVIDUAL PATIENT¿S CONDITION AND OTHER PATIENT SPECIFIC FACTORS. [ALL STENTS MAY BE SUBJECT TO VARYING DEGREES OF ENCRUSTATION WHEN PLACED IN THE URINARY TRACT. ENCRUSTATION MAY RESULT IN OCCLUSION OF THE STENT OR PAIN OR DISCOMFORT FOR THE PATIENT.] <GUIDEWIRE> (1) DO NOT WITHDRAW THE GUIDEWIRE THROUGH A METAL CANNULA OR NEEDLE. EXTREME CAUTION SHOULD BE OBSERVED WHEN USED WITH ONE-WALL PUNCTURE STYLE NEEDLE. [WITHDRAWAL THROUGH A METAL DEVICE MAY RESULT IN DISPOSITION OF THESE MATERIALS IN THE URINARY SYSTEM AND DESTRUCTION AND/OR SEPARATION OF THE OUTER POLYMER JACKET REQUIRING RETRIEVAL.] (2) USE EXTREME CAUTION WHEN USING A LASER OR ELECTROCAUTERY, MAKING SURE TO AVOID CONTACT WITH THE GUIDEWIRE. [DIRECT CONTACT MAY CAUSE DAMAGE TO THE WIRE AND/OR SEVER THE WIRE.] (3) DO NOT USE A TORQUE DEVICE WITH THE GUIDEWIRE. [USE OF A TORQUE DEVICE MAY RESULT IN DAMAGE TO THE WIRE.] (4) DO NOT RESHAPE THE GUIDEWIRE IN ANY WAY. [ATTEMPTING TO RESHAPE THE WIRE MAY CAUSE DAMAGE, RESULTING IN THE RELEASE OF WIRE FRAGMENTS TO THE URINARY SYSTEM.] (5) WHEN EXCHANGING OR WITHDRAWING A CATHETER OVER THE GUIDEWIRE, SECURE AND MAINTAIN THE GUIDEWIRE IN PLACE UNDER FLUOROSCOPY TO AVOID UNEXPECTED GUIDEWIRE ADVANCEMENT. [DAMAGE TO THE URINARY CHANNEL BY THE WIRE¿S TIP MAY OCCUR.] (6) MANIPULATE THE GUIDEWIRE SLOWLY AND CAREFULLY IN THE URINARY SYSTEM WHILE CONFIRMING THE BEHAVIOR AND LOCATION OF THE WIRE¿S TIP UNDER FLUOROSCOPY. IF ANY RESISTANCE IS FELT OR IF THE TIP¿S BEHAVIOR AND/OR LOCATION SEEMS IMPROPER, STOP MANIPULATING THE GUIDEWIRE AND/OR THE CATHETER AND DETERMINE THE CAUSE BY FLUOROSCOPY. IF NECESSARY, REMOVE THE GUIDEWIRE AND ANCILLARY DEVICE OR SCOPE AS A COMPLETE UNIT TO AVOID COMPLICATIONS. [EXCESSIVE MANIPULATION OF THE GUIDEWIRE WITHOUT FLUOROSCOPIC CONFIRMATION MAY RESULT IN PERFORATION OR TRAUMA OF THE LININGS OR ASSOCIATED TISSUES, CHANNELS OR DUCTS. FAILURE TO EXERCISE PROPER CAUTION MAY RESULT IN BENDING, KINKING, AND SEPARATION OF THE GUIDEWIRE¿S TIP, DAMAGE TO THE CATHETER, OR DAMAGE TO THE URINARY SYSTEM.] 2. MALFUNCTION AND ADVERSE EVENTS (1) MALFUNCTION ¿¿FRAGMENTATION, DAMAGE ¿¿GUIDEWIRE KINKING ¿¿DIFFICULTY IN INSERTION ¿¿DIFFICULTY IN REMOVAL ¿¿OCCLUSION ¿¿MIGRATION ¿¿ENCRUSTATION ¿¿DIFFICULTY IN REMOVAL OF THE STENT DUE TO KNOTTING OF THE COIL 1) (2) ADVERSE EVENTS ¿¿EDEMA ¿¿LOSS OF RENAL FUNCTION ¿¿EXTRAVASATION ¿¿PAIN/DISCOMFORT ¿¿FISTULA FORMATION ¿¿PERFORATION OF KIDNEY, RENAL PELVIS, URINARY TRACT AND/OR BLADDER ¿¿HEMORRHAGE ¿¿PERITONITIS ¿¿HYDRONEPHROSIS ¿¿INFECTION ¿¿STONE FORMATION ¿¿URETHRAL EROSION ¿¿URETHRAL REFLUX ¿¿SEPARATED PIECE REMAINING IN BODY ¿¿TISSUE TRAUMA ¿¿URETER AVULSION ¿¿URINARY SYMPTOMS [STORAGE METHOD AND EXPIRATION DATE] 1. STORAGE STORE IN A DRY, COOL PLACE AWAY FROM HEAT, MOISTURE, AND DIRECT SUNLIGHT. 2. EXPIRATION DATE INDICATED ON THE DIRECT PACKAGE AND THE OUTER BOX.¿ H11: SECTION A THROUGH F - THE INFORMATION PROVIDED BY BD REPRESENTS ALL 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. H3 OTHER TEXT : THE ACTUAL/SUSPECTED DEVICE WAS INSPECTED
IT WAS REPORTED THAT THERE WAS A MISPRINT ON THE REIMBURSEMENT CATEGORY ON THE INFORMATION LABEL. THE REDEMPTION CATEGORY PRINTED ON THE BAG INSIDE WHEN THE URETERAL STENT WAS OPENED TO BE USED IN THE OPERATING ROOM SHOULD BE GENERAL I BUT HAS BEEN PRINTED AS GENERAL II. PER ADDITIONAL INFORMATION VIA EMAIL FROM IBC ON 26JAN2022, THIS COMPLAINT WAS AGAINST PRINTING ISSUE ON THE INFORMATION LABEL. SINCE THERE WAS NO PROBLEM TO THE PRODUCT, IT WAS USED.
IT WAS REPORTED THAT THERE WAS A MISPRINT ON THE REIMBURSEMENT CATEGORY ON THE INFORMATION LABEL. THE REDEMPTION CATEGORY PRINTED ON THE BAG INSIDE WHEN THE URETERAL STENT WAS OPENED TO BE USED IN THE OPERATING ROOM SHOULD BE GENERAL I BUT HAS BEEN PRINTED AS GENERAL II. PER ADDITIONAL INFORMATION VIA EMAIL FROM IBC ON 26JAN2022, THIS COMPLAINT WAS AGAINST PRINTING ISSUE ON THE INFORMATION LABEL. SINCE THERE WAS NO PROBLEM TO THE PRODUCT, IT WAS USED.
IT WAS REPORTED THAT THERE WAS A MISPRINT ON THE REIMBURSEMENT CATEGORY ON THE INFORMATION LABEL. THE REDEMPTION CATEGORY PRINTED ON THE BAG INSIDE WHEN THE URETERAL STENT WAS OPENED TO BE USED IN THE OPERATING ROOM SHOULD BE GENERAL I BUT HAS BEEN PRINTED AS GENERAL II. PER ADDITIONAL INFORMATION VIA EMAIL FROM IBC ON (B)(6)2022, THIS COMPLAINT WAS AGAINST PRINTING ISSUE ON THE INFORMATION LABEL. SINCE THERE WAS NO PROBLEM TO THE PRODUCT, IT WAS USED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1080904 | BARD INLAY URETERAL STENT | URETERAL STENT | FAD | C.R. BARD, INC. (COVINGTON) -1018233 | MYEV0960 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown | Other |