NA 7210572Recalls & reported problems
Smith & Nephew, Inc. · ELBOW CONNECTION BAR 2 PER BOX · Class 1
Data updated Oct 13, 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 23596010513827), received between Jun 3, 2020 and Jun 3, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Material Separation” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Material Separation1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 3, 2020Material Separation; Material Separation
IT WAS REPORTED THAT DURING SHOULDER SCOPE THE SURGERY CENTER HAD ISSUES WITH THEIR SHOULDER STABILIZATION KITS. THE COBAN THAT COMES INSIDE THE PACKAGING IS WORTHLESS. IT SHREDS AS SOON AS IT IS USED. IT WAS NOTICED AT THE BEGINNING AND NO DELAY WERE REPORTED. A COMPETITOR DEVICE WAS USED TO COMPLETE THE PROCEDURE. NO OTHER COMPLICATIONS WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10116898 ↗
Other Accessories, operating-room, table (kit) devices
- MAYFIELD® A2101Integra Lifesciences Corporation · Operating Room Accessories Table Tray101 reports
- NA 210080Mako Surgical Corp. · Operating Room Accessories Table Tray74 reports
- ALLEN 104002Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall8 reports
- N/A 7210569Smith & Nephew, Inc. · Accessories, operating-room, table (kit)57 reports
- ALLEN 107004Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall5 reports
- ALLEN 108001Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall3 reports
- NA 7210551Smith & Nephew, Inc. · Accessories, operating-room, table (kit)41 reports
- MAYFIELD® A1018Integra Lifesciences Corporation · Operating Room Accessories Table Tray36 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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