Medline Industries, Inc. DYNJ903942DRecalls & reported problems
Medline Industries, Inc. · NDN CUSTOM BONE RECOVERY · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489700091), received between Sep 23, 2026 and Sep 23, 2026.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
OtherSep 23, 2026Loss of or Failure to Bond
It was reported that "our tissue recovery teams had a number of bags in the bone recovery packs with faulty seals along the bottom."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872090 ↗
Other TRAY, BIOPSY, WITHOUT BIOPSY INSTRUMENTS devices
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- Medline Industries, Inc. DYNJT1911DMedline Industries, Inc. · TRAY, BIOPSY, WITHOUT BIOPSY INSTRUMENTS1 recall0 reports
- ACS MCBP83EAmerican Contract Systems, Inc. · TRAY, BIOPSY, WITHOUT BIOPSY INSTRUMENTS1 recall0 reports
- Medline Industries, Inc. CDS840215OMedline Industries, Inc. · TRAY, BIOPSY, WITHOUT BIOPSY INSTRUMENTS1 recall0 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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