MEDLINE INDUSTRIES DYNJBW25Recalls & reported problems
Medline Industries, Inc. · WAX,BONE,NATURAL · Class U · 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 10080196024216), received between Jun 11, 2018 and Jun 11, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 11, 2018Break
IT WAS REPORTED THAT AT THE BEGINNING OF A STERNOTOMY PROCEDURE A PIECE OF THE BONE WAX BROKE OFF INTO THE SURGICAL SITE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7586478 ↗
Other Wax, bone devices
- ETHICON W31GEthicon, LLC · WAX,BONE20 reports
- Bone Wax BW25GCovidien LP · WAX,BONE3 reports
- Montage 5cc OS-MON-1001Abyrx, Inc. · Wax,Bone2 reports
- MEDLINE BONEWAX YELLOW DYNJBW25Surgical Specialties México, S. de R.L. de C.V. · WAX,BONE1 report
- Permatage 5cc OS-PER-1001Abyrx, Inc. · Wax, Bone1 report
- ETHICON DW31BEthicon Inc. · WAX,BONE1 report
- Ssc Bone Wax 901Surgical Specialties México, S. de R.L. de C.V. · WAX,BONE1 report
- Montage 2cc Multipack OS-MON-1604Abyrx, Inc. · Wax,Bone1 report
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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