FDAClass IINovember 4, 2020

Streamline MIS Navigation System Taps recall

Streamline MIS Navigation System Taps, Catalog Nos. 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN 04-CANNTAP-55-MDN 04-CANNTAP-65-MDN…

Why was Streamline MIS Navigation System Taps recalled?

The Streamline Navigation System taps have experienced binding with other devices.

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?

Lots 377520 371734 374791 374792 373438 371735 371736 377625 377806 371737 372819 371266 371733

Product
Streamline MIS Navigation System Taps, Catalog Nos. 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN 04-CANNTAP-55-MDN 04-CANNTAP-65-MDN…
Recalling firm
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Quantity
420 units
Distribution
US Nationwide distribution including in the state of Michigan.
Recall date
November 4, 2020
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls