Medline Industries, Inc. DYNJRA1740ARecalls & reported problems
Medline Industries, Inc. · 25G WHITACRE SPINAL TRAY · 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
- 4
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10195327088934), received between Mar 24, 2023 and May 29, 2026 — classified as 3 injuries, 1 malfunction.
The most frequently reported specific device problem is “Break” (3 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
- Break3
- Material Integrity Problem1
- Material Twisted/Bent1
Patient problems
- Foreign Body In Patient2
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMay 29, 2026Break; Material Integrity Problem
ACCORDING TO THE FACILITY, ON (B)(6) 2026, CRNA WAS ATTEMPTING TO PLACE A SPINAL BLOCK PRIOR TO A SCHEDULED C-SECTION. THE CRNA FELT A "SNAP/POP" WHILE ATTEMPTING TO GET TO THE CORRECT SPACE, IMMEDIATELY PULLED THE NEEDLE OUT OF THE PATIENT AND NOTED THAT THE NEEDLE HAD BROKEN LEAVING A PORTION OF THE NEEDLE INSIDE THE PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 25334730 ↗InjuryNov 22, 2024Break; Break
ACCORDING TO THE FACILITY, THE WHITACRE NEEDLE WITHIN THE KIT BROKE INSIDE THE PATIENT AND REQUIRED A SECONDARY SURGERY TO RETRIEVE THE NEEDLE FROM THEIR BACK.
Patient problems: Foreign Body In Patient
MAUDE report 20756963 ↗InjuryJun 23, 2023Break; Break
MalfunctionMar 24, 2023Material Twisted/Bent; Material Twisted/Bent
NEEDLE BENT AND ADDITIONAL NEEDLE NEEDED TO BE PLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16610519 ↗
Other Orthopedic tray devices
- Medline Industries, Inc. DYNJ900718CMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ905330BMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ17452SMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ21826RMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. CDS780119VMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ902473LMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ906893DMedline Industries, Inc. · Orthopedic tray4 recalls2 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page