International safety notice

It has been discovered that products with the legal display label of the target lot erroneously affixed at a domestic manufacturing facility may have been shipped to the market. Therefore, we have decided to voluntarily recall the product. is different.

Japan / PMDA Recalls · JPN · Mar 1, 2023

Key facts

Title It has been discovered that products with the legal display label of the target lot erroneously affixed at a domestic manufacturing facility may have been shipped to the market. Therefore, we have decided to voluntarily recall the product. is different.
Regulator Japan / PMDA Recalls
Country JPN
Brand Common name: Internal fixation screw Sales name: Bone Screw Ti
Manufacturer Japan Medical Next Co., Ltd.
Models CO-T2322-S, 511058, 506550
Date Mar 1, 2023
Regulator page info.pmda.go.jp

At a glance

  • No Recall
  • No Field safety notice

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About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

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