[Recalled] Edwards Lifesciences Ergonic Double Acting DeBakey Forceps with Narrow Straight Tip. Model Number ERGF01330. The Edwards Surgical Instruments are designed to perform specialized functions in specific cardiac surgical or endo
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Edwards Lifesciences Ergonic Double Acting DeBakey Forceps with Narrow Straight Tip. Model Number ERGF01330. The Edwards Surgical Instruments are designed to perform specialized functions in specific cardiac surgical or endoscopic procedures. |
|---|---|
| Brand / manufacturer | Edwards Lifesciences, LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0560-2014 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 20 November 2013 |
| EAN / barcode | 11211566 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Edwards Lifesciences is recalling one lot of Ergonic instrument due to mislabeling. Ergonic scissors standard curved labeled as a Double Acting DeBakey forcep. Edwards control confirmed that the laser etching on the device was incorrect.
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 Edwards Lifesciences, LLC
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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