[Recalled] NA-401D-1321 ASPIRATION NEEDLE, model no. NA-401D-1321 - Product Usage: Used with endoscopes to collect cells or tissue specimens in the respiratory organs. — Inspection confirmed a small percentage of sterile packages with inade
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | NA-401D-1321 ASPIRATION NEEDLE, model no. NA-401D-1321 - Product Usage: Used with endoscopes to collect cells or tissue specimens in the respiratory organs. |
|---|---|
| Brand / manufacturer | Aomori Olympus Co., Ltd. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1054-2021 |
| Country of notice | Japan |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 January 2021 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.
This Class II recall concerns device products distributed in Japan and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.