Recall Register

In2Bones, SAS: FDA recalls

FDA enforcement reports name In2Bones, SAS as the recalling firm in 6 events. The events have 10 product records. The recalls started from 2015 to 2024. All the events are device recalls.

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 .

Enforcement events

6 events, newest first.

FDA enforcement events of In2Bones, SAS
InitiatedProduct (first record)TypeClassRecordsStatus
26 Jan 2024I.B.S 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175DeviceClass II2Ongoing
9 Feb 2021In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery.DeviceClass II1Terminated
13 Jul 2017Non-Locking screws in the following lengths: (a) NEO(R) 0.27 - 10 mm, REF W27 ST010 (b) NEO(R) 0.27 - 12 mm, REF W27 ST012 (c) DRP 0.27 - 12 mm, REF W27 ST012 (d) NEO(R) 0.27 - 14 mm, REF W27 ST014 (e) NEO(R) 0.27 - 16 mm, REF W27 ST016 (f) NEO(R) 0.27 - 18 mm, REF W27 ST018 (f) DRP 0.27 - 18 mm, REF W27 ST018 The…DeviceClass II1Terminated
19 Dec 2016SCREW 02.7-12MM LOCKING, REF W27 ST112: a) DRP, b) NEO, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radiusDeviceClass II3Terminated
18 Nov 2015IBS - Osteosynthesis screws for bone fixation Model S25 ST014.DeviceClass II1Terminated
9 Mar 2015DUAFIT(R) PIP 0o CA SIZE 2, REF A60 SP002, STERILE R, Rx only. Interphalangeal implant.DeviceClass II2Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

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

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

Type and class

In2Bones, SAS: events for each product type
TypeEvents
Device6
In2Bones, SAS: events in each class
ClassEvents
Class II6
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
1

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.

Events by year

FDA enforcement events of In2Bones, SAS, by the year that the recall started. The largest year is 2015, with 2 events.

Official channels

Cite this page

Recall Register. In2Bones, SAS: FDA recalls. https://recallregister.com/firm/in2bones-sas/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
N/A

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of In2Bones, SAS have?
Class II: 6 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of In2Bones, SAS?
FDA event 94063, which the firm started on 26 Jan 2024. The first product in the record is: I.B.S 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175
How many FDA recalls of In2Bones, SAS have the status Ongoing?
1 event has the status Ongoing in the openFDA file. openFDA says 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.