Integra JaritRecalls & reported problems across all models
Integra Lifesciences Production Corporation · 57 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 79
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls
- 0
We found 57 models of Integra Jarit by Integra Lifesciences Production Corporation in the FDA's device registry (GUDID). Together they are named in 79 adverse event reports in the FDA's MAUDE database, received between Sep 20, 2019 and Sep 2, 2026 — classified as 11 injuries, 68 malfunctions.
The most frequently reported specific device problem is “Break” (39 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Integra Jarit problems
Device problems
- Break39
- Material Fragmentation8
- Detachment of Device or Device Component7
- Smoking3
- Fracture2
- Material Twisted/Bent2
- Mechanics Altered2
- Overheating of Device2
Patient problems
- No Clinical Signs, Symptoms or Conditions61
- Foreign Body In Patient10
- Insufficient Information3
- Hemorrhage/Blood Loss/Bleeding2
- Abrasion1
- Needle Stick/Puncture1
- No Consequences Or Impact To Patient1
- No Patient Involvement1
Integra Jarit models
57 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Integra® Jarit® 121135HOLDER, NEEDLE, GASTROENTEROLOGIC4 reports
- Integra® Jarit® 600305COAGULATOR-CUTTER, ENDOSCOPIC, UNIPOLAR (AND ACCESSORIES)3 reports
- Integra® Jarit® 600290BELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES3 reports
- Integra® Jarit® 121132INSTRUMENT, MANUAL, SURGICAL, GENERAL USE3 reports
- Integra® Jarit® 275510CUTTER, WIRE3 reports
- Integra® Jarit® 280405RONGEUR3 reports
- Integra® Jarit® 106220HEMOSTAT2 reports
- Integra® Jarit® 106121HEMOSTAT2 reports
- Integra® Jarit® 121186INSTRUMENTS, SURGICAL, CARDIOVASCULAR2 reports
- Integra® Jarit® P6845TCSCISSORS, GENERAL, SURGICAL2 reports
- Integra® Jarit® 101300SCISSORS, OPHTHALMIC2 reports
- Integra® Jarit® 121210HOLDER, NEEDLE, GASTROENTEROLOGIC2 reports
- Integra® Jarit® 275525CUTTER, WIRE2 reports
- Integra® Jarit® 460405DILATOR, TRACHEAL2 reports
- Integra® Jarit® 100262SCISSORS, GENERAL, SURGICAL2 reports
- Integra® Jarit® 285120INSTRUMENT, SURGICAL, NON-POWERED1 report
- Integra® Jarit® 600300COAGULATOR-CUTTER, ENDOSCOPIC, UNIPOLAR (AND ACCESSORIES)1 report
- Integra® Jarit® 600318COAGULATOR-CUTTER, ENDOSCOPIC, UNIPOLAR (AND ACCESSORIES)1 report
- Integra® Jarit® 320185CLAMP, VASCULAR1 report
- Integra® Jarit® 230210RONGEUR1 report
- Integra® Jarit® 605152Laparoscope, general & plastic surgery1 report
- Integra® Jarit® 610107DALaparoscope, general & plastic surgery1 report
- Integra® Jarit® 610165Laparoscope, general & plastic surgery1 report
- Integra® Jarit® 625113Laparoscope, general & plastic surgery1 report
- Integra® Jarit® 625164Laparoscope, general & plastic surgery1 report
- Integra® Jarit® 625090HCOAGULATOR-CUTTER, ENDOSCOPIC, UNIPOLAR (AND ACCESSORIES)1 report
- Integra® Jarit® 600490Laparoscope, general & plastic surgery1 report
- Integra® Jarit® 600340Laparoscope, general & plastic surgery1 report
- Integra® Jarit® 400180SCISSORS, NASAL1 report
- Integra® Jarit® 505232Laparoscope, general & plastic surgery1 report
- Integra® Jarit® 107141HEMOSTAT1 report
- Integra® Jarit® 240124ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Integra® Jarit® 450110RIGAG, MOUTH1 report
- Integra® Jarit® 277274TIINSTRUMENT, MICROSURGICAL1 report
- Integra® Jarit® P14701KNIFE, SURGICAL1 report
- Integra® Jarit® 106171HEMOSTAT1 report
- Integra® Jarit® 205111RETRACTOR1 report
- Integra® Jarit® X21417STRIPPER, VEIN, REUSABLE1 report
- Integra® Jarit® 105161HEMOSTAT1 report
- Integra® Jarit® 120135HOLDER, NEEDLE, GASTROENTEROLOGIC1 report
- Integra® Jarit® 121130INSTRUMENT, MANUAL, SURGICAL, GENERAL USE1 report
- Integra® Jarit® 121140INSTRUMENT, MANUAL, SURGICAL, GENERAL USE1 report
- Integra® Jarit® 121145INSTRUMENT, MANUAL, SURGICAL, GENERAL USE1 report
- Integra® Jarit® 121260TWISTER, WIRE1 report
- Integra® Jarit® 140223FORCEPS, GENERAL & PLASTIC SURGERY1 report
- Integra® Jarit® 225137FORCEPS, GENERAL & PLASTIC SURGERY1 report
- Integra® Jarit® 230261RONGEUR1 report
- Integra® Jarit® 250260OSTEOTOME, MANUAL1 report
- Integra® Jarit® 285391INSTRUMENT, SURGICAL, NON-POWERED1 report
- Integra® Jarit® 400143SPECULUM, ENT1 report
- Integra® Jarit® 106210HEMOSTAT1 report
- Integra® Jarit® 110175HANDLE, SCALPEL1 report
- Integra® Jarit® 130235FORCEPS, GENERAL & PLASTIC SURGERY1 report
- Integra® Jarit® 135181FORCEPS, GENERAL & PLASTIC SURGERY1 report
- Integra® Jarit® 250404MALLET1 report
- Integra® Jarit® 300150RETRACTOR1 report
- Integra® Jarit® 300SRW253RETRACTOR1 report
Recent Integra Jarit adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 2, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50568822 ↗MalfunctionJul 10, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25779680 ↗MalfunctionJun 10, 2026Break
THE FOLLOWING WAS REPORTED VIA MEDWATCH/MDR REPORT # MW:5188148: "DURING A TOTAL HIP REVISION, WHILE ATTEMPTING TO TAKE OUT LINER USING A 1/4 OSTEOTOME, THE OSTEOTOME BROKEN HALF." IT IS UNKNOWN WHETHER PATIENT INJURY OR SURGICAL DELAY OCCURRED; HOWEVER, IT WAS MENTIONED THAT THE FAILURE REQUIRED AN INTERVENTION, AND THE SPECIFICITY OF THE INTERVENTION WAS NOT MENTIONED. NO INITIAL REPORTER DETAILS WERE PROVIDED; THUS, NO REQUEST FOR ADDITIONAL INFORMATION IS POSSIBLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25460678 ↗InjuryMay 29, 2026Break
A FACILITY REPORTED THAT THE BABCOCK TISS FCPS 6-1/4 (135181) WAS BEING USED IN A PROCEDURE WHEN IT BROKE. IT WAS NOT KNOWN AT THE TIME OF SURGERY THAT THE INSTRUMENT HAD BROKEN. THE BREAK WAS DISCOVERED DURING INSTRUMENT CLEANING. ONCE IDENTIFIED, THE PATIENT WAS BROUGHT BACK TO THE OPERATING ROOM FOR A SECOND SURGERY TO RETRIEVE THE RETAINED PIECE. THE BROKEN PART WAS SUCCESSFULLY RECOVERED. NO DEATH OR INJURY WAS REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 25333944 ↗MalfunctionApr 28, 2026Detachment of Device or Device Component
THE FOLLOWING WAS REPORTED VIA MEDWATCH NUMBER (B)(4) THAT DURING A LAPAROSCOPIC OVARIAN CYSTECTOMY, THE COHEN ACORN CANNULA,2-1/8 CERV CONE,LG FOR 505-230 (505232) WAS "FOUND TO BE FUNCTIONAL; HOWEVER, PROPER ENGAGEMENT OF THE CONE TIP REQUIRES A 180-DEGREE TWIST FOR SECURE PLACEMENT. NO ONE NOTICED CONE MISSING FROM DEVICE UPON REMOVAL FROM USE. NO INJURY TO PATIENT, CONE PASSED SPONTANEOUSLY THROUGH VAGINA WHILE URINATING. THE CONE WAS NOT NOTICED TO BE MISSING IN THE OR. PHYSICIAN WAS MADE AWARE BY THE PATIENT AFTER DISCHARGE, WHO THEN ENSURED NO HARM OCCURRED. PATIENT RETURNED CONE TO PHYSICIAN¿S OFFICE DURING FOLLOW UP APPOINTMENT WHO INSPECTED CONE AND DETERMINED IT WAS INTACT. THE CONE WAS NOT RETURNED TO THE HOSPITAL." NO PATIENT INJURY OR DELAY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 25023781 ↗MalfunctionApr 23, 2026Unraveled Material
A FACILITY REPORTED THAT THE CUSTOMER WAS HITTING A PLATE DURING AN ORTHO PROCEDURE; THAT THE JARIT MALLET 2LB SS 7-9/16 (250404) WAS SCORED AND MARKED WHEN USED; THAT SOME MALLETS WERE CHIPPING; AND THAT METAL SHARDS WERE BEING PULLED OUT OF THE PATIENT'S SURGICAL SITE. NO MEDICAL INTERVENTION WAS REQUIRED, AND NO INJURY, DEATH, OR SURGICAL DELAY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24972775 ↗InjuryMar 6, 2026Break
A FACILITY REPORTED THE PRODUCT INSERTS FOR MOUTH GAG (450110RI) WAS TORN, DETACHED, AND WAS FROM THE ELASTIC. IT WAS REPORTED THAT THE SURGEON COMPLETED THE PROCEDURE. UPON REMOVING THE MOUTH GAG, THEY NOTICED THAT ONE OF THE PINS CONNECTING THE ELASTIC TO THE MOUTH GAG HAD TORN/DETACHED FROM THE ELASTIC AND WAS MISSING. THEIR TEAM CONDUCTED A SEARCH IN THE OPERATING ROOM AND INSIDE THE PATIENT¿S MOUTH, BUT THE MISSING PART WAS NOT FOUND. THE PHYSICIAN ALSO EXAMINED THE PATIENT¿S ORAL CAVITY AND DID NOT FIND THE MISSING PIN. ACCORDING TO ONE OF THE TEAMMATES, IT WAS IMPOSSIBLE FOR THE DETACHED PART TO HAVE PASSED THROUGH THE SUCTION. THE PATIENT WAS DISCHARGED HOME FEELING WELL AND WITH NO COMPLAINTS. THERE WAS NO DELAY, INJURY, OR DEATH REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 24531202 ↗MalfunctionMar 3, 2026Break
A FACILITY REPORTED THAT DURING A SEPTOPLASTY AND TURBINECTOMY SURGERY, WHILE USING THE PRODUCT KNIGHT NASAL SCS 7 (400180) FOR THE FIRST TIME, THE SCISSORS SNAPPED IN HALF AT THE HANDLE. ALL BROKEN PARTS WERE RECOVERED AND REMOVED USING A GRASPER. THERE WAS A TWO TO THREE MINUTE DELAY WHILE RETRIEVING AND REPLACING THE BROKEN SCISSORS. THERE WAS NO PATIENT INJURY OR DEATH, AND THE PATIENT WAS UNDER ANESTHESIA WHEN THE BREAK OCCURRED. THE PROCEDURE WAS SUCCESSFULLY COMPLETED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24495772 ↗MalfunctionJan 12, 2026Break
THE FOLLOWING WAS REPORTED VIA MEDWATCH/MDR REPORT # MW5179561: "DURING A SCHEDULED SURGERY OF LEFT DISTAL RADIUS OPEN REDUCTION INTERNAL FIXATION ON, SURGEON ATTEMPTED TO USE A WIRE CUTTER TO TRIM A METAL WIRE AND UNEXPECTEDLY THEY STATED THAT THE WIRE CUTTER'S BLADE SCATTERED INTO MULTIPLE PIECES AND FELL INTO PATIENT'S SURGICAL SITE." ATTEMPTS HAVE BEEN MADE TO OBTAIN ADDITIONAL INFORMATION REGARDING THE SELECTION CLINICAL CODE: ALTERED STATE OF CONSCIOUS IN VOLUNTARY MEDWATCH REPORT. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24036583 ↗InjuryOct 16, 2025Break; Break
A FACILITY REPORTED THAT THE RHOTON-TYPE BALL DISS 71/2 90D TT (277274TI) INSTRUMENT BROKE AT A 90-DEGREE ANGLE AT THE TIP AND WAS LEFT IN THE PATIENT. ACCORDING TO ADDITIONAL INFORMATION RECEIVED FROM THE STERILE PROCESSING SUPERVISOR, IT WAS NOTED THAT THE NEUROSURGERY RESIDENT AND THE OPERATING ROOM TEAM WHO WORKED ON THE CASE STATED THAT THE BROKEN PART WAS NOT RECOVERED, AND THE FLUOROSCOPY X-RAY THAT WAS PERFORMED DID NOT DETECT ANY BROKEN PIECES. IT WAS ALSO CONVEYED THAT THE PATIENT WAS UNDER GENERAL ANESTHESIA DURING THE PROCEDURE, AND THE OPERATING ROOM TEAM TRIED TO RETRIEVE THE BROKEN PIECE AFTER "COMMITTING A SIGNIFICANT AMOUNT OF TIME TRYING TO TAKE THE BROKEN PIECE OUT, " BUT IT WAS UNSUCCESSFUL. ACCORDING TO THE NEUROSURGERY RESIDENT, THE PIECE MIGHT HAVE BEEN SUCTIONED OUT WHEN HE WAS DISSECTING TO REMOVE IT, AND THE PATIENT WAS NOTIFIED OF THE INCIDENT." A DIFFERENT INSTRUMENT THAT WAS AVAILABLE WAS USED TO COMPLETE THE SURGERY. POSTOPERATIVELY, THE PATIENT HAD THE SURGERY ON (B)(6) 2025, WAS DISCHARGED ON (B)(6) 2025, AND HAD A RE-ADMISSION DUE TO A COMPLAINT OF NECK PAIN ON (B)(6) 2025 AND DISCHARGED ON (B)(6) 2025.
Patient problems: Foreign Body In Patient
MAUDE report 23318716 ↗MalfunctionSep 10, 2025Smoking; Smoking
MalfunctionJul 14, 2025Break; Break
A FACILITY REPORTED THAT DURING A TOTAL KNEE REPLACEMENT, THE OCHSNER FCPS 8 STR SATIN (106220) BROKE AT THE JAW. THE BROKEN JAW WAS RECOVERED, AND ANOTHER INSTRUMENT WAS USED TO COMPLETE THE SURGERY. NO INJURIES, DEATHS, OR SURGICAL DELAYS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22501491 ↗MalfunctionJul 7, 2025Break; Break
A FACILITY REPORTED THAT DURING A CARDIAC PROCEDURE, THE JAWS OF THE 5-1/2 CURVED SATIN CRILE FORCEPS (106121) BROKE OFF INTO THE PATIENT'S OPERATIVE SITE. THE BROKEN PART WAS RETRIEVED. NO PATIENT INJURY, DEATH, OR SURGICAL DELAY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22420413 ↗MalfunctionJul 3, 2025Break; Break
A FACILITY REPORTED THAT DURING A CARDIAC PROCEDURE, THE JAWS OF THE 5-1/2 CURVED SATIN CRILE FORCEPS (106121) BROKE OFF INTO THE PATIENT'S OPERATIVE SITE. THE BROKEN PART WAS RETRIEVED. NO PATIENT INJURY, DEATH, OR SURGICAL DELAY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22392006 ↗InjuryJul 1, 2025Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
IT WAS REPORTED THAT THE 5MM 45CM SLIDE LOCK HUNTER BOWEL GRASPER (610165) WAS MISSING THE SCREW THAT SECURES IT TO THE LARYNGOSCOPE. ADDITIONALLY, A PORTION OF THE INSTRUMENT BROKE OFF INSIDE THE PATIENT DURING LAPAROSCOPIC GENERAL SURGERY. AT THIS TIME, IT IS UNKNOWN WHETHER THE BROKEN PART WAS RETRIEVED. NO FURTHER PATIENT CONSEQUENCE WAS REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 22376357 ↗
Other Integra Lifesciences Production Corporation products
All Integra Lifesciences Production Corporation devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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