ConMed 50L abdominal insufflator recall
ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expanded cavity (pneumoperitoneum)…
Why was ConMed 50L abdominal insufflator recalled?
An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.
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?
Lot Codes: 9855JEG to 93879JEG
- Product
- ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expanded cavity (pneumoperitoneum)…
- Recalling firm
- Northgate Technologies, Inc.
- Quantity
- 25 units
- Distribution
- US Nationwide distribution in the states of FL and OH.
- Recall date
- March 3, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)