International safety notice
It was discovered that the expiration date of the product in question was incorrectly displayed on the label, which was longer than the correct expiration date. We have decided to voluntarily recall the affected products.
Japan / PMDA Recalls · JPN · Oct 23, 2023
Key facts
| Title | It was discovered that the expiration date of the product in question was incorrectly displayed on the label, which was longer than the correct expiration date. We have decided to voluntarily recall the affected products. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: Single Use Class III Treatment Kit Sales name: Medline Surgical Custom Kit Surgical use |
| Manufacturer | Medline Japan LLC |
| Models | KS2398727, KS2285088, KS2388192, M19RAD004A, M32GAL001D, M34RAD003A, KS2388519, M01RAD013A, KS2287357, KS2388959, KS2388625, M01CAR013B and 2 more |
| Date | Oct 23, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
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