Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
Reported: March 5, 2014 Initiated: December 16, 2013 #Z-1080-2014
Product Description
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
Reason for Recall
During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 284
- Distribution
- Nationwide Distribution.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 284.
Why was this product recalled? ▼
During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 5, 2014. Severity: Moderate. Recall number: Z-1080-2014.
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