NuOss 5099104Recalls & reported problems
Ace Surgical Supply CO., Inc. · NUOSS CANCELLOUS 2GRAM/6.8CC PARTICLE SIZE 1-2MM · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00614950007516), received between Dec 27, 2017 and Dec 27, 2017 — classified as 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
- Patient-Device Incompatibility1
Patient problems
- Inflammation2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 27, 2017Patient-Device Incompatibility
PATIENT EXPERIENCED SWELLING WITHIN 24 HOURS OF PROCEDURE, NO INFECTION WAS OBSERVED. THE PATIENT RECEIVED ANTIBIOTICS, PAIN MEDICATION AND MOUTHWASH. THE SYMPTOMS SUBSIDED WITHIN 1 WEEK.
Patient problems: Inflammation
MAUDE report 7148264 ↗InjuryDec 27, 2017Insufficient Device Problem Information
PATIENT EXPERIENCED SWELLING WITHIN 24 HOURS OF PROCEDURE, NO INFECTION WAS OBSERVED. THE PATIENT RECEIVED ANTIBIOTICS, PAIN MEDICATION AND MOUTHWASH. THE SYMPTOMS SUBSIDED WITHIN 1 WEEK.
Patient problems: Inflammation
MAUDE report 7148262 ↗
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- 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 5099002Ace Surgical Supply CO., Inc. · BONE GRAFTING MATERIAL, ANIMAL SOURCE3 reports
- NuOss 5099100Ace 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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