MinerOss XP MINXP-CAN0.5SMRecalls & reported problems
Collagen Matrix, Inc. · Porcine Anorganic Bone Mineral 0.5cc (Particle Size 0.25 - 1.0 mm) · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813954021645), received between Mar 24, 2025 and Mar 24, 2025 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- No Apparent Adverse Event1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 24, 2025No Apparent Adverse Event; No Apparent Adverse Event
COLLAGEN MATRIX, INC. RECEIVED MEDWATCH FORM MW5166536-1 FROM THE FDA ON 02/17/2025. THE FORM INDICATES THAT ON (B)(6) 2024, THE PATIENT HAD AN ALLOGRAFT DONE AT AN UNKNOWN SITE/LOCATION. SINCE THEN, THE PATIENT CONTRACTED TUBERCULOSIS (TB) AND HAS BEEN WORKING WITH PHYSICIANS TO GET ON A 9-MONTH ANTIBIOTIC REGIMEN. SINCE THE LAST TIME THE PATIENT TESTED NEGATIVE FOR TB. THE ONLY OTHER PERSON THE PATIENT HAD SUBSTANTIAL CONTACT WITH HAS RECENTLY TESTED NEGATIVE FOR TB. AS A RESULT, IT IS SUSPECTED THAT THE ALLOGRAFT TO BE THE MEANS BY WHICH THE PATIENT CONTRACTED TB. IN THE INITIAL MEDWATCH FORM, THE FOLLOWING PRODUCTS WERE INDICATED AS FOLLOWS: INFORMATION ABOUT THE COMPANIES INVOLVED IN PROVIDING THE BONE TISSUE USED IN (B)(6) ALLOGRAFT: MINEROSS XP, REF: MINXPCAN0.5SM LOT PMCU23K1; USE BY 2026-08-31 MANUFACTURER: COLLAGEN MATRIX INC. DISTRIBUTED BY (B)(4) LOT: FG24030528, CORTICAL AND CANCELLOUS CHIPS 1.0CC QUALITY DEPARTMENT (B)(6). CADAVER BONE TISSUE IMPLANTED IN ALLOGRAFT. COLLAGEN MATRIX, INC. REACHED OUT TO THE INITIAL COMPLAINANT THAT OUR PRODUCT IS A XENOGRAFT (PORCINE ANORGANIC BONE MINERAL) AND NOT AN ALLOGRAFT INITIALLY INDICATED IN THE MEDWATCH FORM. ADDITIONAL INFOR
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 21677347 ↗
Other Bone Grafting Material, Animal Source devices
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- NuOss 5091003Ace Surgical Supply CO., Inc. · BONE GRAFTING MATERIAL, ANIMAL SOURCE1 recall0 reports
- Gibson Healthcare® Bone Graft Plug 5824-413Collagen Matrix, Inc. · Bone Grafting Material, Animal Source6 reports
- OSSIX™ Bone 0.250 ccDatum Dental Ltd · Bone Grafting Material, Animal Source5 reports
- NuOss 5091004Ace Surgical Supply CO., Inc. · BONE GRAFTING MATERIAL, ANIMAL SOURCE5 reports
- PreservaRidge™ Plug PRPREGCollagen Matrix, Inc. · Bone Grafting Material, Animal Source3 reports
- NuOss 5099100Ace Surgical Supply CO., Inc. · BONE GRAFTING MATERIAL, ANIMAL SOURCE3 reports
- NuOss 5099002Ace Surgical Supply CO., Inc. · BONE GRAFTING MATERIAL, ANIMAL SOURCE3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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