International safety notice
For K-NOA DOAM, which we manufacture and sell, the chemical immersion time is listed in the approval form as part of the surface treatment conditions. As it was discovered that the product had been shipped for less than the specified time, we have decided to voluntarily recall the product with the lot number. did.
Japan / PMDA Recalls · JPN · May 9, 2023
Key facts
| Title | For K-NOA DOAM, which we manufacture and sell, the chemical immersion time is listed in the approval form as part of the surface treatment conditions. As it was discovered that the product had been shipped for less than the specified time, we have decided to voluntarily recall the product with the lot number. did. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: spinal cage Sales name: K-NOA DOAM Alkaline Porous Spacer |
| Manufacturer | Osaka Yakin Kogyo Co., Ltd. |
| Models | 722980, 722104, 722081, 722040, 722102, 722039, 722067, 722066, 722140, 722059, 722038, 722078 and 9 more |
| Date | May 9, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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