International safety notice
This product is used by attaching it to the brooch handle, but the dimensions of the attachment part are slightly small in some parts of this product, and the brooch handle is attached to the handle. We have internally confirmed that there is a possibility that the product may not mate with the roach handle, so we have decided to carry out a voluntary recall. did.
Japan / PMDA Recalls · JPN · Sep 24, 2024
Key facts
| Title | This product is used by attaching it to the brooch handle, but the dimensions of the attachment part are slightly small in some parts of this product, and the brooch handle is attached to the handle. We have internally confirmed that there is a possibility that the product may not mate with the roach handle, so we have decided to carry out a voluntary recall. did. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Joint surgical instruments Brand name: Hip joint surgical instruments |
| Manufacturer | Microport Orthopedics Japan Co., Ltd. |
| Models | PRGLBR08, CN103328, PRGLBR04, CN103235, PRGLBR03, PRGLBR02, PRGLBR09, CN103250, CN103205, PRGLBR10, PRGLBR06 |
| Date | Sep 24, 2024 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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