Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RAPIDSORB IPS Battery Pack Recalled by Synthes (USA) Products LLC Due to Products not sterilized, sterility cannot be confirmed
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 Synthes (USA) Products LLC directly.
Affected Products
RAPIDSORB IPS Battery Pack, Sterile-Intended for use in non-load bearing fracture repair and reconstructive procedures of the craniofacial skeleton (excluding the upper and lower jaw) in pediatric and adult populations. Part Number: 530.553.01S
Quantity: 10 units
Why Was This Recalled?
Products not sterilized, sterility cannot be confirmed
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Synthes (USA) Products LLC
Synthes (USA) Products LLC has 162 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report