Medline Industries, Inc. DYNJ36775ARecalls & reported problems
Medline Industries, Inc. · C SECTION PACK-LF · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884389718988), received between Jun 16, 2025 and Jun 17, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (3 reports).
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
- Patient Device Interaction Problem3
Patient problems
- Rash3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 17, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryJun 17, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryJun 16, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
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- Medline Industries, Inc. DYNJ9932207RMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ69445Medline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ904653GMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ15494GMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ33059BMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ47808FMedline Industries, Inc. · Cesarean section tray3 recalls0 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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