Medtronic Curved Suction 90 9733451 EM ENT recall
Medtronic Curved Suction 90 9733451 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction…
Why was Medtronic Curved Suction 90 9733451 EM ENT recalled?
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
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 numbers 17030728, 17022027, 17021426, 17013125, 17012724, 17011303, 16122767, 16122066, 16112965, and 16112164
- Product
- Medtronic Curved Suction 90 9733451 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction…
- Recalling firm
- Medtronic Navigation, Inc.
- Quantity
- 75 instruments
- Distribution
- Worldwide Distribution - US (nationwide) and Internationally to Canada.
- Recall date
- August 30, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)