[Recalled] PrepStain Syringing Pipettes 240 (Catalog #490517) — The PrepStain Syringing Pipettes may not dispense the minimum volume of 7.5 mL… | FDA 2012-03-22
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | PrepStain Syringing Pipettes 240 (Catalog #490517) |
|---|---|
| Brand / manufacturer | Tripath Imaging, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1811-2012 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 22 March 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The PrepStain Syringing Pipettes may not dispense the minimum volume of 7.5 mL of the sample due to leaking. This event resulted in an increase in complaints of leaking syringing pipettes
This Class III 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 →
Related recalls from Tripath Imaging, Inc.
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.
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