Non-Locking Screw, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label. Size (Part Number): a) D 2.0MM X 8MM (0002-D-20008); b) D 2.0MM X 10MM (002-D-20010); c) D 2.0MM X 12MM (002-D-20012); d) D 2.0MM X 14MM (002-D-20014); e) D 2.0MM X 16MM (002-D-20016); f) D 2.0MM X 18MM (002-D-20018); g) D 2.0MM X 20MM (002-D-20020); h) D 2.0MM X 22MM (002-D-20022); i) D 2.0MM X 24MM (002-D-20024); j) D 2.0MM X 26MM (002-D-20026); k) D 2.0MM X 28MM (002-D-20028); l) D 2.0MM X 30MM (002-D-20030)
Class I - DangerousWhat Should You Do?
- Check if you have this product: (UDI)/Lot: a) (18056099645614) B1204542, B1101808; b) (18056099645621) B1204969, B1201169, B1075101; c) (18056099645638) B1204554, B1195701, B1075428; d) (18056099645645) B1204971, B1201176, B1075846; e) (18056099645652) B1195727, B1204266, B1075426; f) (18056099645669) B1204540, B1075429; g) (18056099645676) B1204541, B1075425; h) (18056099645683) B1204539, B1075177; i) (18056099645690) B1204972, B1195700, B1075847; j) (18056099645706) B1204555, B1195702, B1075427; k) (18056099645713) B1204973, B1201170, B1075430; l) (18056099645720) B1075825, B1201166, B1204270
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Orthofix, Inc
- Reason for Recall:
- Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating System and Rival View Plating System. As the result of a complaint investigation, the locking screws were confirmed to not properly engage the plates during surgery.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Non-Locking Screw, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label. Size (Part Number): a) D 2.0MM X 8MM (0002-D-20008); b) D 2.0MM X 10MM (002-D-20010); c) D 2.0MM X 12MM (002-D-20012); d) D 2.0MM X 14MM (002-D-20014); e) D 2.0MM X 16MM (002-D-20016); f) D 2.0MM X 18MM (002-D-20018); g) D 2.0MM X 20MM (002-D-20020); h) D 2.0MM X 22MM (002-D-20022); i) D 2.0MM X 24MM (002-D-20024); j) D 2.0MM X 26MM (002-D-20026); k) D 2.0MM X 28MM (002-D-20028); l) D 2.0MM X 30MM (002-D-20030)
Product Codes/Lot Numbers:
(UDI)/Lot: a) (18056099645614) B1204542, B1101808; b) (18056099645621) B1204969, B1201169, B1075101; c) (18056099645638) B1204554, B1195701, B1075428; d) (18056099645645) B1204971, B1201176, B1075846; e) (18056099645652) B1195727, B1204266, B1075426; f) (18056099645669) B1204540, B1075429; g) (18056099645676) B1204541, B1075425; h) (18056099645683) B1204539, B1075177; i) (18056099645690) B1204972, B1195700, B1075847; j) (18056099645706) B1204555, B1195702, B1075427; k) (18056099645713) B1204973, B1201170, B1075430; l) (18056099645720) B1075825, B1201166, B1204270
Distribution:
Distributed in: NJ, FL, PA, SC, LA, VA, MN, TX, GA, DC, NV, IN, CA, MI, IL, MD, NC, OH, OK
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2119-2018
Related Recalls
Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating System and Rival View Plating System. As the result of a complaint investigation, the locking screws were confirmed to not properly engage the plates during surgery.
Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating System and Rival View Plating System. As the result of a complaint investigation, the locking screws were confirmed to not properly engage the plates during surgery.
Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating System and Rival View Plating System. As the result of a complaint investigation, the locking screws were confirmed to not properly engage the plates during surgery.