Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with Recalled by Aesculap, Inc. Due to Certain lots of the Aesculap Hi Line XXS...
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 Aesculap, Inc. directly.
Affected Products
Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN¿ and microspeed motor systems to hold burrs which cut and shape bone.
Quantity: 14
Why Was This Recalled?
Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were recalled due to a possible failure of the handpiece.
Where Was This Sold?
This product was distributed to 4 states: NY, PA, TN, TX
About Aesculap, Inc.
Aesculap, Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report