Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product recall
Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the…
Why was Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product recalled?
The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial Number 7621683
- Product
- Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the…
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 1
- Distribution
- US Nationwide distribution in the states of CT, IL, MN, MO, and NC.
- Recall date
- March 20, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)