[Recalled] Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory. Model numbers: PP-5.75-90 PP-9-90 PP-5.75-90PL PP-9-90PL — Identification of packaging breach of the nylon pouch sterile barrier for the 3… | FDA 2014
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory. Model numbers: PP-5.75-90 PP-9-90 PP-5.75-90PL PP-9-90PL |
|---|---|
| Brand / manufacturer | ORIGIO, Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1946-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 20 June 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Identification of packaging breach of the nylon pouch sterile barrier for the 3-pack configuration
This Class II recall concerns device products distributed in United States 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 →
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.