Mammotrak Interventional Coil 3.0T
Reported: December 4, 2024 Initiated: November 4, 2024 #Z-0544-2025
Product Description
Mammotrak Interventional Coil 3.0T
Reason for Recall
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Details
- Recalling Firm
- Philips North America Llc
- Units Affected
- 5,231 units
- Distribution
- US Nationwide distribution.
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
Mammotrak Interventional Coil 3.0T. Recalled by Philips North America Llc. Units affected: 5,231 units.
Why was this product recalled? ▼
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 4, 2024. Severity: Moderate. Recall number: Z-0544-2025.
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