Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation Recalled by Stryker GmbH Due to The wrong parts were picked for packaging. 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 Stryker GmbH directly.
Affected Products
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults.
Quantity: 18
Why Was This Recalled?
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker GmbH
Stryker GmbH has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report