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[Recalled] Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine. — The graphics at the attachment interface indicating locked and unlocked positio… | FDA 201

recall fda device united-states

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductAnspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine.
Brand / manufacturerThe Anspach Effort, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2253-2016
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date15 June 2016

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The graphics at the attachment interface indicating locked and unlocked position are reversed.

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 The Anspach Effort, 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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