Medline Industries, Inc. PAIN0072KRecalls & reported problems
Medline Industries, Inc. · PAIN MGMT/ PREF W. MED NDL · Class 2
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 10889942694754), received between May 15, 2024 and May 15, 2024 — 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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 15, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON 04/19/2024 "THE 27G NEEDLE FROM THE PAIN TRAY WAS INSERTED INTO THE PATIENT'S LOWER BACK, THE NEEDLE WAS INSERTED UP TO THE HUB AND WHEN THE PHYSICIAN ATTEMPTED TO ADJUST THE NEEDLE FROM THE SIDE TO SIDE THE NEEDLE BROKE OFF OF THE HUB".
Patient problems: Foreign Body In Patient
MAUDE report 19320813 ↗
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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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