Medtronic ANGLED DRILL recall
Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
Why was Medtronic ANGLED DRILL recalled?
Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than what is indicated on the print specification.
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?
UDI: 00643169363502, Lot Number EM17F015
- Product
- Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
- Recalling firm
- Medtronic Sofamor Danek USA Inc
- Quantity
- 2 units
- Distribution
- MN, NC
- Recall date
- February 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)