PRECICE Intramedullary Limb Lengthening SystemRecalls & reported problems across all models
Nuvasive Specialized Orthopedics, Inc. · 551 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name at least one PRECICE Intramedullary Limb Lengthening System model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 177
- Deaths reported
- 0
- Injuries reported
- 61
- Recalls
- 4
We found 551 models of PRECICE Intramedullary Limb Lengthening System by Nuvasive Specialized Orthopedics, Inc. in the FDA's device registry (GUDID). Together they are named in 177 adverse event reports in the FDA's MAUDE database, received between Apr 14, 2016 and May 27, 2026 — classified as 61 injuries, 116 malfunctions.
The most frequently reported specific device problem is “Failure to Advance” (51 reports).
4 FDA recall records name at least one of these models by its device identifier, 4 still open.
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
PRECICE Intramedullary Limb Lengthening System recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Oct 29, 2021Open, Classified
The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing treatment, and (3) That no more than two devices should be implanted at a time.
Z-0319-2022 · Root cause: Device Design · names 549 of these models · Recall details · FDA record ↗
- Feb 12, 2021Open, Classified
Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.
Z-1351-2021 · Root cause: Device Design · names 66 of these models · Recall details · FDA record ↗
- Feb 12, 2021Open, Classified
Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.
Z-1350-2021 · Root cause: Device Design · names 104 of these models · Recall details · FDA record ↗
- Feb 12, 2021Open, Classified
Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.
Z-1349-2021 · Root cause: Device Design · names 498 of these models · Recall details · FDA record ↗
Most reported PRECICE Intramedullary Limb Lengthening System problems
Device problems
- Failure to Advance51
- Break46
- Mechanical Problem19
- Fracture18
- Material Twisted/Bent14
- Defective Device13
- Detachment of Device or Device Component8
- Migration5
Patient problems
- Failure of Implant108
- No Clinical Signs, Symptoms or Conditions46
- Pain10
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available5
- Implant Pain5
- Metal Related Pathology5
- No Code Available5
- Bone Fracture(s)4
PRECICE Intramedullary Limb Lengthening System models
551 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- PRECICE® Intramedullary Limb Lengthening System LSC5-075Rod, Fixation, Intramedullary And Accessories4 recalls2 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-045Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- PRECICE® Intramedullary Limb Lengthening System LSC5-050Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- PRECICE® Intramedullary Limb Lengthening System LSC5-020Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-025Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-030Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-035Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-040Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-055Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-060Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-065Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-070Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-020Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-025Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-030Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-035Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-040Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-045Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-050Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-055Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-060Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-065Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-070Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-075Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-080Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-085Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-090Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-095Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-100Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-065Rod, Fixation, Intramedullary And Accessories3 recalls1 report
- PRECICE® Intramedullary Limb Lengthening System TSA5-075Rod, Fixation, Intramedullary And Accessories3 recalls1 report
- PRECICE® Intramedullary Limb Lengthening System CPA2-005Rod, Fixation, Intramedullary And Accessories3 recalls1 report
- PRECICE® Intramedullary Limb Lengthening System CPA1-000Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-020Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-025Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-030Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-035Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-040Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-045Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-050Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-055Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSB3-060Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-020Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-025Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-030Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-035Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-040Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-045Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-050Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-055Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System LSC4-060Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-020Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-022.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-025Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-027.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-030Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-032.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-035Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-037.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-040Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-042.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-045Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-047.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-050Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-055Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-060Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-070Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-080Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-085Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-090Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-095Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA5-100Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-020Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-025Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-030Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-035Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-040Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-045Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-050Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-055Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE Intramedullary Limb Lengthening System LSB4-060Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-020Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-022.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-025Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-027.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-030Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-032.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-035Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-037.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-040Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-042.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-045Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-047.5Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-050Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-055Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-060Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-065Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-070Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-075Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
- PRECICE® Intramedullary Limb Lengthening System TSA4-080Rod, Fixation, Intramedullary And Accessories3 recalls0 reports
Recent PRECICE Intramedullary Limb Lengthening System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionMay 27, 2026Failure to Advance
IT WAS REPORTED THAT A PRECICE NAIL WAS IMPLANTED IN (B)(6) ON A STATURE PATIENT. HIS RIGHT SIDE LENGTHENED BUT THE LEFT NAIL DID NOT. THE PATIENT LOST FAITH IN HIS ORIGINAL SURGEON, SO HE CAME TO (B)(6) TO HAVE DR. (B)(6) SWAP OUT THE NAIL. THE NAIL DID WORK ON THE BACK TABLE WITH A FAST DISTRACTOR, BUT (B)(6) STILL WANTED US TO SWAP IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25306652 ↗MalfunctionMay 18, 2026Positioning Failure
IT WAS REPORTED THAT A PATIENT HAD A LEFT FEMORAL LENGTHENING PROCEDURE WHERE 8 CM LENGTHENING WAS PLANNED VIA NUVASIVE PRECICE MAGNETIC NAIL WHICH WAS PLANNED. AFTER BRIEFLY GAPPING 5 MM, NAIL FAILED TO LENGTHEN AND DETERMINED TO BE DEVICE FAILURE. A REVISION SURGERY PERFORMED WITH NEW NAIL PLACED.
Patient problems: Failure of Implant
MAUDE report 25204460 ↗MalfunctionFeb 17, 2026Break; Fracture
IT WAS REPORTED THAT THE PRECICE NAIL WAS DISCOVERED AS CRACKED DURING THE EXTRACTION SURGERY, WE ARE UNCERTAIN AT THIS STAGE WHETHER THE CRACK OCCURRED BEFORE OR DURING EXTRACTION, CURRENT UNDERSTANDING IS THAT IT DID NOT AFFECT THE PATIENT'S SURGICAL OUTCOME. THIS EVENT OCCURRED IN UK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24369924 ↗MalfunctionFeb 9, 2026Positioning Failure
IT WAS REPORTED THAT DURING A SURGERY TO RECHARGE THE PRECICE NAIL NEITHER THE FAST DISTRACTOR MAX NOR THE ERC WERE ABLE TO RETRACT THE NAIL DESPITE NUMEROUS ATTEMPTS. THE ERC SHOWED THERE WAS A CONNECTION BETWEEN MAGNETS WITH A GREEN CHECK MARK BUT THERE WAS NO ACTUAL MOVEMENT OF THE NAIL. THE NAIL WAS THEN REMOVED AND TESTED ON THE BACK TABLE WITH NO SUCCESS. THE NAIL HAD BEEN EXTRACTED TO 78 MM PRIOR TO THE RECHARGE SURGERY. POST-OP, THE PATIENT REPORTED THAT DURING HIS FINAL DISTRACTIONS WITH THE ERC VIA THE PRESCRIPTION HE WAS HEARING A CLUNKING SOUND. HIS PRESCRIBED TREATMENT WAS .33 MM X 3 TIMES A DAY.
Patient problems: Failure of Implant
MAUDE report 24295164 ↗MalfunctionJan 9, 2026Material Twisted/Bent
IT WAS REPORTED BY THE SURGEON THAT THE PRECICE NAIL IS VERY BENT AND REQUIRES REVISION SURGERY TO REPLACE NAIL. THE NAIL REMAINS IN SITU WITH PLAN FOR REMOVAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24021669 ↗MalfunctionDec 18, 2025Fracture; Fracture
IT WAS REPORTED THAT A PRECICE NAIL WAS IMPLANTED ON (B)(6) 2022. ON (B)(6) 2025, THE PATIENT WAS ADMITTED FOR AN OSTEOTOMY DUE TO THE BREAKAGE OF THE PRECICE SCREW AND THE DISTAL AND PROXIMAL SCREWS. FRAGMENTS EXTRACTED, AND NAIL WAS REPLACED.
Patient problems: Failure of Implant
MAUDE report 23842504 ↗MalfunctionDec 16, 2025Break; Fracture; Break; Fracture
IT WAS REPORTED THAT THE PATIENT UNDERWENT PRECICE HARDWARE EXCHANGE DUE TO A BROKEN NAIL. THE PATIENT REQUIRED AN OSTEOTOMY TO FIX THE MALROTATION OF FEMUR.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 23818463 ↗MalfunctionDec 15, 2025Break; Failure to Advance; Break; Failure to Advance
THE PATIENT HAD BILATERAL FEMUR PRECICE NAILS IMPLANTED ON (B)(6) 2025. THE NAIL IN THE LEFT FEMUR WAS NOT LENGTHENING SO DR. (B)(6) REPLACED THE NON-FUNCTIONING PRECICE NAIL WITH A NEW ONE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23810092 ↗MalfunctionDec 12, 2025Failure to Advance; Failure to Advance
IT WAS REPORTED THAT A PRECICE NAIL WAS IMPLANTED IN (B)(6) ON A STATURE PATIENT. HIS RIGHT SIDE LENGTHENED BUT THE LEFT NAIL DID NOT. THE PATIENT LOST FAITH IN HIS ORIGINAL SURGEON, SO HE CAME TO (B)(6) TO HAVE DR. (B)(6) SWAP OUT THE NAIL. THE NAIL DID WORK ON THE BACK TABLE WITH A FAST DISTRACTOR, BUT (B)(6) STILL WANTED US TO SWAP IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23790510 ↗MalfunctionDec 2, 2025Failure to Advance; Failure to Advance
IT WAS REPORTED THAT THE ORIGINAL SURGERY WAS PERFORMED IN OCTOBER, ON (B)(6) 2025. IT WAS A BILATERAL SURGERY AND TWO NAILS WERE IMPLANTED. ONE WAS WORKING AND THE OTHER WASN'T, SO IN NOVEMBER, ON (B)(6) 2025, SURGERY WAS PERFORMED TO REMOVE THE MALFUNCTIONING NAIL AND IMPLANT ANOTHER. THIS EVENT OCCURRED IN SPAIN.
Patient problems: Failure of Implant
MAUDE report 23697362 ↗MalfunctionNov 13, 2025Failure to Advance; Failure to Advance
IT WAS REPORTED THAT A REVISION SURGERY TO REPLACE A PRECICE NAIL THAT WAS NOT LENGTHENING OCCURRED.
Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions
MAUDE report 23548062 ↗MalfunctionNov 13, 2025Break; Fracture; Break; Fracture
NAIL STARTED TO BEND POST OP DURING PATIENT LENGTHENING AND EVENTUALLY BROKE. NAIL WAS REMOVED AND REPLACED WITH TRAUMA NAIL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23545214 ↗MalfunctionNov 10, 2025Failure to Advance; Failure to Advance
PRECICE NAIL WAS TESTED WITH FAST DISTRACTOR, AND THE NAIL DID NOT MOVE. WE TRIED SEVERAL TIMES AND SUDDENLY THE THINNER PART OF THE NAIL PLOBBED OUT ABOUT 2CM. AFTER THAT, YOU COULD BY HAND MOVE THE THINNER PART OF THE NAIL BACK AND FORTH. THE NAIL WAS REPLACED WITH A NEW WORKING PRECICE NAIL WITH REPORTED GOOD OUTCOME. THIS REVISION TOOK PLACE ON (B)(6) 2025. THIS EVENT OCCURRED IN GERMANY.
Patient problems: Failure of Implant
MAUDE report 23513257 ↗MalfunctionNov 3, 2025Failure to Advance; Failure to Advance
IT WAS REPORTED THAT THE PRECICE NAIL IMPLANTATION WAS ON (B)(6) 2025. AFTER 2 WEEKS THE X-RAYS SHOWED NO MOVEMENT OF THE NAIL. REVISION SURGERY WAS ON (B)(6) 2025. THE NAIL DID NOT TRANSPORT IN SITU BUT DID EX SITU.
Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions
MAUDE report 23457929 ↗MalfunctionNov 3, 2025Fracture; Fracture
PATIENT OF 15 YEARS OLD DID FALL AND BREAK HIS BONE INCLUDING THE PRECICE NAIL IN THIS EVENT. REVISION HAS TAKEN PLACE ON (B)(6) 2025 WITH A STD TRAUMA NAIL. THE LENGTHENING HAS BEEN ACHIEVED WITH THE PRECICE NAIL. THEREFORE, A TRAUMA NAIL HAS BEEN PLACED FOR HEALING AFTER THE BREAK CAUSED BY THE PATIENT'S FALL. THIS EVENT TOOK PLACE IN THE NETHERLANDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23455532 ↗
Other Nuvasive Specialized Orthopedics, Inc. products
- MAGEC Spinal Bracing and Distraction System29 models · 663 reports · 1 recall
- PRECICE STRYDE System231 models · 139 reports · 2 recalls
- PRECICE Bone Transport System561 models · 28 reports · 3 recalls
- PRECICE Plating System67 models · 24 reports · 3 recalls
- PRECICE Trauma Nail System182 models · 4 reports · 3 recalls
- FREEDOM Residual Limb Lengthening System2 models · 1 reports · 2 recalls
- Precice38 models · 9 reports · 1 recall
- PRECICE System15 models · 0 reports · 1 recall
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.
How reports and recalls are matched · Editorial policy · Report an error on this page