Overview of recall records associated with Medtronic Sofamor Danek USA, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 66.
This lot has incorrectly been laser marked both on the screw head itself as well as the data carrier tag attached to the screw. The description on face two of the screw head and on the data…
The firm received complaints of drill bits breaking during use with the Prestige LP(TM) Cervical Disc System. Subsequent investigation demonstrated the interaction of the drill guide and…
Slot screw had an overall length of 15mm, but per the specification, the screw should have an overall length of approximately 17mm.
Medtronic has discovered the directional arrow at the proximal end of the instrument may not correctly align with the cut out opening on the distal end of the instrument.
The directional arrow at the proximal end of the instrument may not correctly align with the cutout opening on the distal end of the instrument. Using affected bone void filler may result…
Product packaging may incorrectly include two bevel-tipped needles or two trocar-tipped needles instead of one diamond-tipped needle and one bevel-tipped needle.
The dovetails of poly trials, Beta 2.0, were observed as either cracked or broken.
The dovetails of poly trials, Beta 2.0, were observed as either cracked or broken.
The dovetails of poly trials, Beta 2.0, were observed as either cracked or broken.
The dovetails of poly trials, Beta 2.0, were observed as either cracked or broken.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
This page summarizes recall records in which the official source identifies Medtronic Sofamor Danek USA, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
