Z-1526-2018 Class II Terminated
FDA device recall Z-1526-2018 was initiated by Stryker GmbH on Mar 12, 2018 and is designated Class II. Reason for recall: The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling The recall status is terminated (terminated May 21, 2020). Affected quantity: 18.
Recall Details
- Product Type
- Devices
- Report Date
- May 2, 2018
- Initiation Date
- Mar 12, 2018
- Termination Date
- May 21, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 18
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
Distribution Pattern
USA (nationwide) Distribution
Code Information
Lot # L23745
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1526-2018
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026