Pair of leg plates 113373BCRecalls & reported problems
MAQUET GmbH · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04046768073296), received between Dec 21, 2023 and Dec 21, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information3
- Use of Device Problem3
Patient problems
- Laceration(s)3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 21, 2023Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information
ON 12TH DECEMBER 2023, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF THE ACCESSORIES - 113373BC - PAIR OF LEG PLATES, 4-PART USED WITH 720001B2 - MEERA EU WITH AUTO DRIVE. AS IT WAS STATED, THE USER CUT THEIR INDEX FINGER WHEN REMOVING THE LEG PLATES. ACCORDING TO PROVIDED INFORMATION, THE CUT WAS SUPERFICIAL AND ONLY THE PLASTER WAS APPLIED. NO STITCHES WERE NECESSARY. WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE USER'S BODY CUT DURING USE OF THE LEG PLATE, WAS TO REOCCUR.
Patient problems: Laceration(s)
MAUDE report 18380603 ↗MalfunctionDec 21, 2023Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information
MalfunctionDec 21, 2023Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information
Other TABLE AND ATTACHMENTS, OPERATING-ROOM devices
- Arthrex® AR-1747-BArthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM12 reports
- Arthrex® AR-1644Arthrex, Inc. · Table and attachments, operating-room5 reports
- Leg holder 100380A0MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM4 reports
- Arthrex® AR-1560-02Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM4 reports
- Arthrex® AR-1500Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM3 reports
- Traction boot, adult 10018800MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 reports
- Arthrex® AR-1646Arthrex, Inc. · Table and attachments, operating-room2 reports
- Seat plate extension 116055DCMAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 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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