Medline Industries, Inc. DYNJRA9038Recalls & reported problems
Medline Industries, Inc. · TRAY, 24G WHIT SPINAL W/PHARM · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10193489830477), received between Feb 15, 2023 and Oct 18, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Integrity Problem” (2 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Apr 10, 2026Class IOpen, Classified
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
Z-2237-2026 · Root cause: Component design/selection · Recall details · FDA record ↗
Most reported problems
Device problems
- Material Integrity Problem2
Patient problems
- Foreign Body In Patient1
- Foreign Body Reaction1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 18, 2023Material Integrity Problem; Material Integrity Problem
THE CUSTOMER REPORTED, "A PIECE OF THE NEEDLE BROKE OFF AND WAS EMBEDDED IN THE PATIENT REQUIRING THE PATIENT TO HAVE IT SURGICALLY REMOVED".
Patient problems: Foreign Body Reaction
MAUDE report 17958503 ↗InjuryFeb 15, 2023Material Integrity Problem; Material Integrity Problem
ACCORDING TO THE FACILITY ON 01/19/23 "THE HUB OF THE INTRODUCER NEEDLE CAME CLEAN OFF OF THE NEEDLE UPON GENTLE PRESSURE TO REMOVE THE HUB AFTER THE SPINAL WAS PLACED".
Patient problems: Foreign Body In Patient
MAUDE report 16382773 ↗
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- Medline Industries, Inc. DYNJ909505AMedline Industries, Inc. · Orthopedic tray4 recalls1 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 · each recall links to the FDA recall notice
- 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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