Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled by Zimmer Biomet, Inc. Due to Spin Down RapidFlap nut that interfaces with the...
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 Zimmer Biomet, Inc. directly.
Affected Products
Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1030-12 Used for the re-attachment of the bone flap after a craniotomy.
Quantity: 11580 units
Why Was This Recalled?
Spin Down RapidFlap nut that interfaces with the outer plate was assembled incorrectly.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report