[Recalled] Carefusion V. Mueller GERALD BIPOLAR FORCEPS 1.0MM WIDE TIP OVERALL LENGTH 7" (17.8CM) , REF F-1110 — BD has determined that the Instructions For Use (IFU) provided by BD is missing… | FDA 2022-11-02
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Carefusion V. Mueller GERALD BIPOLAR FORCEPS 1.0MM WIDE TIP OVERALL LENGTH 7" (17.8CM) , REF F-1110 |
|---|---|
| Brand / manufacturer | Carefusion 2200 Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0380-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 02 November 2022 |
| EAN / barcode | 10885403040771 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface with the device power supply, as well as cleaning and maintenance instructions. Refer to the attached V. Mueller" Bipolar Forcep IFU.
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 →
Related recalls from Carefusion 2200 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.