FDA Device recall Z-1964-2016
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses
- FDA Device
- Class II
- terminated
- Published 2016-06-22
On 2016-06-22 the FDA classified a Class II recall of STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses by Staar Surgical, citing the STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1964-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-02 |
| Published | 2016-06-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Staar Surgical |
| Distribution | n/a |
Product
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
Reason
The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).
Identifiers
| code_info | 1281706, 1282812 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Other recalls by Staar Surgical
- EVO +VISIAN Implantable Collamer Lens, REF: VICM5_13.7.Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical - EVO+VISIAN Implantable Collamer Lens, REF: VTICM5_12.1. Phakic Toric Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical - EVO VISIAN Implantable Collamer Lens, REF: VICMO12.1. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical - EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical - EVO VISIAN Implantable Collamer Lens, REF: VICMO12.6. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1964-2016%22
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