BostonSight PROSE Lens.
Reported: August 6, 2025 Initiated: June 10, 2025 #Z-2191-2025
Product Description
BostonSight PROSE Lens.
Reason for Recall
Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.
Details
- Recalling Firm
- Boston Foundation For Sight
- Units Affected
- 38 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada.
- Location
- Needham, MA
Frequently Asked Questions
What product was recalled? ▼
BostonSight PROSE Lens.. Recalled by Boston Foundation For Sight. Units affected: 38 units.
Why was this product recalled? ▼
Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 6, 2025. Severity: Moderate. Recall number: Z-2191-2025.
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