Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

ANSPACH Recalled by The Anspach Effort, Inc. Due to Certain lots of the Otologic Curved Micro (OCM)...

Date: March 28, 2016
Company: The Anspach Effort, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact The Anspach Effort, Inc. directly.

Affected Products

ANSPACH, Rx only, Otologic Curved Micro (OCCM) Diamond Ball Burr, 1.5 MM, Part # OCM7-15SD Product Usage: The Otologic Curved Micro (OCCM) Attachment and burrs are intended for cutting and shaping bone primarily in otology procedures such as cochleostomies.

Quantity: 27 devices

Why Was This Recalled?

Certain lots of the Otologic Curved Micro (OCM) Diamond Ball Burrs may be missing the diamond coating and the ball may be the incorrect size.

Where Was This Sold?

This product was distributed to 2 states: KY, TX

Affected (2 states)Not affected

About The Anspach Effort, Inc.

The Anspach Effort, Inc. has 261 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report