ErgoJust LTM & ICU IP-EC-VIDEO-EXTRecalls & reported problems
Xltek · IP PTZ ErgoJust Video Extension · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00382830058377), received between Aug 16, 2023 and Jan 18, 2024 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Crack” (8 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
- Crack8
- Unintended Movement6
- Break1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 18, 2024Crack; Unintended Movement; Crack; Unintended Movement
IP PTZ ERGOJUST VIDEO EXTENSION -VIDEO EXTENSIONS ON 6 OF 7 CART PURCHASED IN 2021 HAVE CRACKS. CAMERA ARMS ARE BREAKING OFF. NO INJURIES. EVENT: 6/6.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18533342 ↗MalfunctionJan 18, 2024Crack; Unintended Movement; Crack; Unintended Movement
IP PTZ ERGOJUST VIDEO EXTENSION -VIDEO EXTENSIONS ON 6 OF 7 CART PURCHASED IN 2021 HAVE CRACKS. CAMERA ARMS ARE BREAKING OFF. NO INJURIES. EVENT: 5/6
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18533341 ↗MalfunctionJan 18, 2024Crack; Unintended Movement; Crack; Unintended Movement
IP PTZ ERGOJUST VIDEO EXTENSION -VIDEO EXTENSIONS ON 6 OF 7 CART PURCHASED IN 2021 HAVE CRACKS. CAMERA ARMS ARE BREAKING OFF. NO INJURIES. EVENT: 4/6.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18533338 ↗MalfunctionJan 18, 2024Crack; Unintended Movement; Crack; Unintended Movement
IP PTZ ERGOJUST VIDEO EXTENSION -VIDEO EXTENSIONS ON 6 OF 7 CART PURCHASED IN 2021 HAVE CRACKS. CAMERA ARMS ARE BREAKING OFF. NO INJURIES. EVENT: 3/6.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18533283 ↗MalfunctionJan 18, 2024Crack; Unintended Movement; Crack; Unintended Movement
IP PTZ ERGOJUST VIDEO EXTENSION -VIDEO EXTENSIONS ON (B)(4) CART PURCHASED IN 2021 HAVE CRACKS. CAMERA ARMS ARE BREAKING OFF. NO INJURIES. EVENT: 2/6.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18533279 ↗MalfunctionJan 18, 2024Crack; Unintended Movement; Crack; Unintended Movement
IP PTZ ERGOJUST VIDEO EXTENSION -VIDEO EXTENSIONS ON 6 OF 7 CART PURCHASED IN 2021 HAVE CRACKS. CAMERA ARMS ARE BREAKING OFF. NO INJURIES. EVENT: 1/6.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18533275 ↗MalfunctionOct 5, 2023Crack; Crack
IP PTZ ERGOJUST VIDEO EXTENSION: ARM TO CAMERA HAS BROKEN. THE CUSTOMER SAID THAT THIS ACTUALLY HAPPENED WHILE THE TECHNICIAN WAS PUSHING IT DOWN THE HALLWAY. NO ONE WAS HURT OR INJURED DURING THE EVENT. HE STATED HE NOTICED IT FALLING DOWN AND CAUGHT IT AND HELD IT UP UNTIL HE GOT BACK INTO THE DEPARTMENT. THE CUSTOMER PROVIDED PICTURES OF THE DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17877524 ↗MalfunctionAug 16, 2023Break; Crack; Material Twisted/Bent; Break; Crack; Material Twisted/Bent
IP PTZ ERGOJUST VIDEO EXTENSION - CART HAS CRACKED VIDEO EXTENSION. PICTURES PROVIDED OF THE FAILURE WERE REVIEWED AND IT WAS NOTED THE BRACKET DOES NOT LOOK TO BE INSTALLED ON THE CUSTOMER'S EQUIPMENT. NO INJURIES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17554904 ↗
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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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