International safety notice
There was a report that an identification label indicating product number 0112-20J was affixed to the outer box of this product 0110-20J. Product and legal display label 0110-20J Attached identification label 0112-20J As a result of the investigation, it was found that the packaging, labeling, and storage manufacturing facility in Japan was involved in the packaging, labeling, and storage of the packaged products during the work on the lot. It was confirmed that a different identification label for product number 0112-20J was attached, so the lot was voluntarily recalled. That's it. A legal label is affixed to the outer box, but the product number written on the legal label is Consistent with the product.
Japan / PMDA Recalls · JPN · Dec 13, 2021
Key facts
| Title | There was a report that an identification label indicating product number 0112-20J was affixed to the outer box of this product 0110-20J. Product and legal display label 0110-20J Attached identification label 0112-20J As a result of the investigation, it was found that the packaging, labeling, and storage manufacturing facility in Japan was involved in the packaging, labeling, and storage of the packaged products during the work on the lot. It was confirmed that a different identification label for product number 0112-20J was attached, so the lot was voluntarily recalled. That's it. A legal label is affixed to the outer box, but the product number written on the legal label is Consistent with the product. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Short-term use gastrostomy feeding tube Brand name: MIC● Feeding tube (● indicates an asterisk) |
| Manufacturer | Avanos Medical Japan Inc. |
| Models | 0110-20J, 30138225 |
| Date | Dec 13, 2021 |
| 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