Truliant, Activit-ERecalls & reported problems across all models
Exactech, Inc. · 48 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Truliant, Activit-E model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls
- 1
We found 48 models of Truliant, Activit-E by Exactech, Inc. in the FDA's device registry (GUDID). Together they are named in 9 adverse event reports in the FDA's MAUDE database, received between Aug 9, 2024 and Sep 24, 2026 — classified as 9 injuries.
The most frequently reported specific device problem is “Unstable” (3 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 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
Truliant, Activit-E 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.
- Nov 21, 2023Open, Classified
Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Z-0586-2024 · Root cause: Packaging change control · names 42 of these models · Recall details · FDA record ↗
Most reported Truliant, Activit-E problems
Device problems
- Adverse Event Without Identified Device or Use Problem5
- Unstable3
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
- Patient-Device Incompatibility1
Patient problems
- Joint Laxity3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Fall1
- Insufficient Information1
- Joint Dislocation1
- Unspecified Infection1
- Wound Dehiscence1
Truliant, Activit-E models
48 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Truliant, Activit-E 02-023-02-0035PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall1 report
- Truliant, Activit-E 02-024-35-2510Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall1 report
- Truliant, Activit-E 02-024-44-3009PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall1 report
- Truliant, Activit-E 02-023-02-0029PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-023-02-0032PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-023-02-0038Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-1512Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-1515Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-1519PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-2010PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-2013PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-2015PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-2509Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-2511PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-2512PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-3010PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-3012PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-3013Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-3513Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-3515Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-4012PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-4013Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-4510PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-4515Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-5011Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-35-5012PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-1511Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-2009PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-2011PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-2015Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-2510PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-2515Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-3011Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-3013PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-3015Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-3509PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-4009PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-4509PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-44-4511Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-4512Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-4513Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 recall0 reports
- Truliant, Activit-E 02-024-44-5013PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Truliant, Activit-E 02-024-35-4009Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Truliant, Activit-E 02-024-35-5009PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Truliant, Activit-E 02-024-51-1513PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Truliant, Activit-E 02-024-51-3013PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Truliant, Activit-E 02-024-51-3509PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Truliant, Activit-E 02-024-51-4010Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
Recent Truliant, Activit-E adverse event reports
The 9 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 24, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Wound Dehiscence
MAUDE report 50884624 ↗InjuryJul 1, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THIS PATIENT UNDERWENT A LEFT KNEE REPLACEMENT. SUBSEQUENTLY, THEY DEVELOPED AN INFECTION. THE SURGEON WASHED OUT THE JOINT AND EXCHANGED THE POLY. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Unspecified Infection
MAUDE report 25680627 ↗InjuryMay 13, 2026Unstable
IT WAS REPORTED THAT A PATIENT WHO HAD A RIGHT TKA, UNDERWENT A REVISION PROCEDURE DUE TO AN UNSTABLE KNEE. THE PATIENT WAS SIZED UP TO A SIZE 3 X 13 CRC POLY. THERE WERE NO DEVICE BREAKAGES OR SURGICAL DELAYS DURING THE PROCEDURE. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. X-RAYS WERE PROVIDED. THE EXPLANTED DEVICES ARE NOT AVAILABLE FOR RETURN AS THEY WERE THROWN OUT BY THE HOSPITAL. NO DEVICE IMAGES WERE PROVIDED. NO FURTHER INFORMATION.
Patient problems: Joint Laxity
MAUDE report 25161546 ↗InjuryMar 31, 2026Patient-Device Incompatibility; Device Dislodged or Dislocated
IT WAS REPORTED THAT A 72 Y) FEMALE PATIENT, WHO HAD A LEFT TKA, UNDERWENT A REVISION PROCEDURE. THE PATELLA WAS NOT TRACKING PROPERLY. THERE WERE NO DEVICE BREAKAGES OR SURGICAL DELAYS DURING THE PROCEDURE. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO FURTHER INFORMATION.
Patient problems: Joint Dislocation
MAUDE report 24747010 ↗InjuryJan 21, 2026Unstable
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL TOTAL KNEE ARTHROPLASTY ON THE LEFT SIDE. SUBSEQUENTLY, THE PATIENT EXPERIENCED INSTABILITY. AS A RESULT, THE SURGEON DID A POLY SWAP AND INCREASED THE POLY THICKNESS TO A 4X11MM PS POLY. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO FURTHER INFORMATION AVAILABLE.
Patient problems: Joint Laxity
MAUDE report 24130000 ↗InjuryAug 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL TOTAL KNEE REPLACEMENT ON THE LEFT SIDE. SUBSEQUENTLY, THE PATIENT EXPERIENCED A FALL THAT WAS NOT ATTRIBUTED TO INSTABILITY. AS A RESULT, THE PATIENT UNDERWENT A REVISION. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO FURTHER IMPACT TO THE PATIENT WAS REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: Fall
MAUDE report 22908795 ↗InjuryMar 11, 2025Unstable; Unstable
IT WAS REPORTED THAT THIS PATIENT'S LEFT KNEE WAS REVISED APPROXIMATELY 1 YEAR 3 MONTH POST INITIAL OPERATION. PATIENT FELT UNSTABLE SO THE SURGEON INCREASED POLY THICKNESS TO 13MM. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.
Patient problems: Joint Laxity
MAUDE report 21573086 ↗InjurySep 17, 2024Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
IT WAS REPORTED THAT THIS FEMALE PATIENT'S RIGHT KNEE WAS REVISED APPROXIMATELY 2 MONTHS POST OP. THE PATIENT WAS BROUGHT BACK FOR A RIGHT KNEE IRRIGATION AND DEBRIDEMENT AND POLY SWAP. THE POLY LINER WAS REMOVED WITH THE HELP OF AN OSTEOTOME. AFTER IRRIGATION AND DEBRIDEMENT WAS FINISHED A NEW 1.5 13MM CRC WAS IMPLANTED WITH 20CC INTERSEP. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. PRODUCT NOT RETURNING: ITEM WAS DISCARDED.
Patient problems: Insufficient Information
MAUDE report 20241190 ↗InjuryAug 9, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT, INITIAL RIGHT KNEE IMPLANTED IN (B)(6) 2024, UNDERWENT A REVISION PROCEDURE IN (B)(6) 2024, APPROXIMATELY 4 MONTHS POST THE INITIAL PROCEDURE. THE PATIENT DEVELOPED SOFT TISSUE ADHESIONS. THE PATIENT HAD A MANIPULATION UNDER ANESTHESIA WITH NO SUCCESS. THEY THEN UNDERTOOK A SURGICAL APPROACH TO FREE UP THE ADHESIONS AND PERFORMED A POLY EXCHANGE. LIKELY THEY WERE REMOVING THE POLY TO IMPROVE EXPOSURE AND AS IT¿S SINGLE USE HAD TO REPLACE WITH A NEW ONE. THERE DOESN¿T APPEAR TO BE ANY ALLEGED DEFECT WITH THE DEVICE. THERE WERE NO ISSUES WITH THE SURGERY. THE REP WILL TRY TO RETRIEVE THE DEVICE TO RETURN FOR ANALYSIS. A DEVICE IMAGE WAS PROVIDED. NO FURTHER INFORMATION.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 19954462 ↗
Other Exactech, Inc. products
- Equinoxe305 models · 2,076 reports · 37 recalls
- Optetrak Logic408 models · 3,306 reports · 3 recalls
- Novation184 models · 1,145 reports · 25 recalls
- Optetrak336 models · 1,773 reports · 6 recalls
- Truliant414 models · 1,010 reports · 2 recalls
- Acumatch A Series94 models · 54 reports · 15 recalls
- MCS25 models · 7 reports · 5 recalls
- Alteon135 models · 100 reports · 3 recalls
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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