Alteon Neck Preserving Stem, Standard Offset, Plasma Coated, Size 6
Reported: January 25, 2017 Initiated: November 7, 2016 #Z-1032-2017
Product Description
Alteon Neck Preserving Stem, Standard Offset, Plasma Coated, Size 6
Reason for Recall
Products were labeled with incorrect Global Trade Item Numbers. The GTIN on the label identifies the devices as another.
Details
- Recalling Firm
- Exactech, Inc.
- Units Affected
- 98
- Distribution
- AZ, CA, CO, FL, IL, KS, MD, NJ, NY, OH, OK, TN, & VA; Germany, Italy, Japan, Spain, & Switzerland.
- Location
- Gainesville, FL
Frequently Asked Questions
What product was recalled? ▼
Alteon Neck Preserving Stem, Standard Offset, Plasma Coated, Size 6. Recalled by Exactech, Inc.. Units affected: 98.
Why was this product recalled? ▼
Products were labeled with incorrect Global Trade Item Numbers. The GTIN on the label identifies the devices as another.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 25, 2017. Severity: Moderate. Recall number: Z-1032-2017.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11