RecallRadar

FDA Device recall Z-0408-2018

smith&nephew, 2.4 MM, 6 HOLE, EVOS, FLEX PLATE, SST Plate, REF CATALOG NUMBER 72442360N, NON-STERILE, Rx only, (01)00885556456446(10), (11)…

On 2018-01-31 the FDA classified a Class II recall of smith&nephew, 2.4 MM, 6 HOLE, EVOS, FLEX PLATE, SST Plate, REF CATALOG NUMBER 72442360N, NON-STERILE, Rx only, (01)00885556456446(10), (11)… by Smith And Nephew, citing one lot of EVOS 2.4MM Flex Plate 6 Hole packaging contained templates.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0408-2018
ClassificationClass II
Statusterminated
Initiated2017-11-29
Published2018-01-31
Last updated2026-09-13 11:54 UTC
CompanySmith And Nephew
DistributionOR

Product

smith&nephew, 2.4 MM, 6 HOLE, EVOS, FLEX PLATE, SST Plate, REF CATALOG NUMBER 72442360N, NON-STERILE, Rx only, (01)00885556456446(10), (11)171116 Bone plates and bone screws from the EVOS Mini-Fragment Plating System are intended for use in internal fixation of small bones and small bone fragments and non-load bearing stabilization and reduction of bone fragments in long bones.

Reason

One lot of EVOS 2.4MM Flex Plate 6 Hole packaging contained templates.

Identifiers

code_info17AM14602

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0408-2018%22

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