Wright Medical Recalls Swanson Finger Joint Implants Due to Sterility Documentation Issues
Wright Medical Technology is recalling 20 units of Swanson Finger Joint #1 implants because documentation confirming sterility was inadequate.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text explicitly states the issue is a lack of documentation confirming sterility without reporting any illnesses or injuries, fitting the criteria for a voluntary precautionary recall or minor documentation issue.
Plain-English summary
Wright Medical Technology, Inc. is recalling 20 units of the SWANSON FINGER JOINT #1, Part Number 4700001. The recall affects Lot Number 1555726. The firm discovered a lack of adequate documentation confirming sterility on these specific products.
The affected devices were distributed in the United States and internationally, including Norway, Italy, Germany, France, South Africa, the UK, Taiwan, Austria, Japan, Turkey, Denmark, Canada, Switzerland, Belgium, The Netherlands, and Spain. The source text does not specify the exact number of patients affected or report any illnesses or injuries.
Consumers and healthcare providers should contact Wright Medical Technology, Inc. for further instructions regarding the return or replacement of these devices.
The recalled product
- Product
- SWANSON FINGER JOINT #1, Part Number 4700001
- Manufacturer
- Wright Medical Technology, Inc.
- Hazard
- Affected units
- 20
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Number 1555726
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 12 recalled by Wright Medical Technology, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 12 products in this recall →Related recalls
Same manufacturer · Wright Medical Technology, Inc.
See all →- HighStryker Infinity Resection Adjustment Block Recall: Missing Locking Screw
FDA (Devices) · 2024-04-10
- HighStryker Infinity Alignment Frame Distal Sub-Assembly Recalled for Manufacturing Defect
FDA (Devices) · 2023-07-12
- HighStryker ORTHOLOC 3Di Fusion Plate Contains Incorrect Laser Markings
FDA (Devices) · 2023-05-03
- HighStryker ORTHOLOC 3Di Fusion Plate Recalled for Incorrect Marked Descriptions
FDA (Devices) · 2023-05-03
- HighBone fixation plates recalled due to product packaging mix-up
FDA (Devices) · 2023-03-08
Same hazard · sterility documentation
See all →- ModerateWright Medical Recalls PRO-STIM Injectable Due to Sterility Documentation Issues
FDA (Devices) · 2019-12-04
- ModerateWright Medical Recalls Ortholoc 3DI Locking Screws Due to Sterility Documentation Issues
FDA (Devices) · 2019-12-04
- ModerateWright Medical Recalls Swanson Trapezium Implants Due to Sterility Documentation Issues
FDA (Devices) · 2019-12-04
- ModerateWright Medical Recalls Evans Opening Wedge Plates Due to Sterility Documentation
FDA (Devices) · 2019-12-04
- ModerateWright Medical Recalls Valor Screws Due to Sterility Documentation Issues
FDA (Devices) · 2019-12-04