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.
Reported: May 2, 2018 Initiated: March 12, 2018 #Z-1526-2018
Product Description
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.
Reason for Recall
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
Details
- Recalling Firm
- Stryker GmbH
- Units Affected
- 18
- Distribution
- USA (nationwide) Distribution
- Location
- Selzach, N/A
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Stryker GmbH. Units affected: 18.
Why was this product recalled? ▼
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 2, 2018. Severity: Moderate. Recall number: Z-1526-2018.
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