Reported Jun 22, 2016 · Terminated
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
Staar Surgical Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Staar Surgical Co. · 1911 Walker Ave · Monrovia, CA · 91016-4846
Is this the product you have?
- STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
- Lot codes and dates
12817061282812
- Amount recalled
- 2,612 units
Why it was recalled
The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Staar Surgical Co. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.