FDA Device recall Z-2153-2015
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
- FDA Device
- Class II
- terminated
- Published 2015-07-29
On 2015-07-29 the FDA classified a Class II recall of Bausch & Lomb SofPort Advanced Optics Aspheric Lens by Bausch And Lomb Surgical, citing haptics breaking during lens loading and insertion.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2153-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-26 |
| Published | 2015-07-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Bausch And Lomb Surgical |
| Distribution | US |
Product
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Reason
Haptics breaking during lens loading and insertion.
Identifiers
| code_info | Produce Code: LI61AO and LI61SE. LOT #'s 4455501 4455723 4456117 4456118 4456123 4456207 4456213 4456214 445…Produce Code: LI61AO and LI61SE. LOT #'s 4455501 4455723 4456117 4456118 4456123 4456207 4456213 4456214 4456306 4456316 4456318 4456319 4456403 4456406 4456412 4456413 4456414 4456415 4456416 4456703 4456704 4456707 4456710 4456711 4456712 4456713 4456714 4456715 4456716 4456717 4456718 4456719 4456720 4456721 4456722 4456723 4456724 4456725 4456726 4456727 4456801 4456803 4456804 4456805 4456807 4456808 4456809 4456810 4456811 4456812 4456813 4456814 4456815 4456816 4456817 4456818 4456819 4456820 4456821 4456822 4456823 4456824 4456825 4456826 4456827 4456828 4456829 4456830 4456831 4456832 4456901 4456902 4456903 4456904 4456905 4456906 4456907 4456908 4456909 4456910 4456911 4456912 4457001 4457002 4457003 4457004 4457005 4457006 4457007 4457008 4457009 4457010 4457011 4457012 4457013 4457014 4457015 4457016 4457017 4457018 4457019 4457020 4457021 4457022 4457101 4457102 44 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2153-2015%22
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