[Recalled] ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery. — High friction of the slider can cause the device to stick, or not move as inten… | FDA 2022-03-16

Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: High friction of the slider can cause the device to stick, or not move as intended.

This Class II recall concerns device products distributed in Germany 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.