Z-2253-2016 Class II Terminated
FDA device recall Z-2253-2016 was initiated by The Anspach Effort, Inc. on Jun 15, 2016 and is designated Class II. Reason for recall: The graphics at the attachment interface indicating locked and unlocked position are reversed. The recall status is terminated (terminated Dec 14, 2016). Affected quantity: 18.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 27, 2016
- Initiation Date
- Jun 15, 2016
- Termination Date
- Dec 14, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 18
Product Description
Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine.
Reason for Recall
The graphics at the attachment interface indicating locked and unlocked position are reversed.
Distribution Pattern
Worldwide Distribution: US Distribution to states of: GA and FL; and country of: Switzerland.
Code Information
Lot #'s: H29309439804, H44310033104, K09311396703, and K09311396704.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2253-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026