Fluoroscopy systems recalled over ceiling suspension screws that may loosen
Canon Medical Systems is recalling 332 Alphenix INFX-8000V systems because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 because the record's stated consequences are loss of movement, noise and a sensor error, with no patient harm or reported injury.
Plain-English summary
The Alphenix INFX-8000V interventional fluoroscopic x-ray system is being recalled by Canon Medical System, USA, INC.
The record states it has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. The record states that as a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed.
The record lists 332 units, with serial numbers recorded in the enforcement record. Distribution was worldwide, covering the United States nationwide and the Dominican Republic. The FDA has classified the action as Class II.
The stated consequences in the enforcement record are loss of lateral movement, abnormal noise and a sensor error, and no injuries are reported. Facilities should follow Canon's instructions.
The recalled product
- Product
- Roasted Pumpkin & White Cheddar Tamales Ingredients: Organic Corn Flour Masa, Pumpkin, Green Chile, Sharp Cheddar Cheese (Pasteurized Milk, Cheese Cultures, Salt and Enzymes), Butter, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and Mon
- Manufacturer
- Prima Vera Nueva, Inc.
- Category
- Medical Device — Fluoroscopy
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- UPC: 748732000263
Distribution
Part of a larger recall action
This product is one of 10 recalled by Prima Vera Nueva, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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