FDAClass IIJune 18, 2014

Lindemann Drill Short recall

Lindemann Drill Short, 1.6mm Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery…

Why was Lindemann Drill Short recalled?

There may be missing notches, partial notches or no notches at all in some Cutting Accessories that are used with the Elite" Attachments.

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?

Part Number 5820-102-16, Lot Number 14006017

Product
Lindemann Drill Short, 1.6mm Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery…
Recalling firm
Stryker Instruments Div. of Stryker Corporation
Quantity
12
Distribution
Worldwide Distribution - US (nationwide)
Recall date
June 18, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls