Recall Register

Device recall: Invue Solid Driver, Tipped, AO. Part Number: 11-70083. Allows the user to retain the screw when changing axis of…

Class II FDA enforcement event 64994. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

The nipple of the tipped driver broke off when surgeons were attempting to insert the screw.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

SpineFrontier, Inc. started this device recall on 9 May 2012. The firm address in the FDA record is in Beverly, MA. FDA put the recall in Class II. FDA event 64994 has 1 product record. The first FDA enforcement report date is 21 Aug 2013. The record gives the status Terminated, with the termination date 10 Jan 2014.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Distributed in DC and the states of MA, and OK.

Recalling firm

SpineFrontier, Inc., Beverly, MA.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 64994: product records
Recall numberProductQuantityClassStatusReport date
Z-1957-2013Invue Solid Driver, Tipped, AO. Part Number: 11-70083. Allows the user to retain the screw when changing axis of insertion during fixation of spinal intervertebral.9Class IITerminated21 Aug 2013

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2012
823
Share of these events in Class II
88%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
26

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 64994. https://recallregister.com/fda/ii/64994/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Distributed in DC and the states of MA, and OK.
What quantity of product is in FDA event 64994?
The FDA record gives this quantity: 9
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2012 have the same class?
88% of the 823 device events that started in 2012 are in Class II.