CLASS II ONGOING Device recall · Reported 15 Mar 2017 · FDA Enforcement Report

Color contact lenses labeled under the following brands recalled

The See Clear is recalling Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, distributed nationwide in the US. The recall was initiated on 6 Jan 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots of lenses sold between 10/31/2013 to 10/31/2016

Quantity recalled119,829 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1404-2017
FDA event ID: 76279
Recalling firm: The See Clear, Peachtree Corners, GA
Classification: Class II
Status: Ongoing
Recall initiated: 6 Jan 2017
FDA classified: 3 Mar 2017
Reported: 15 Mar 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Labeling Errors
Device type: Contact Lenses & Eye Devices

Timeline

6 Jan 2017	Recall initiated by company
3 Mar 2017	Classified by FDA	+56 days
15 Mar 2017	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Sterility and Misbranding: Lenses may not be sterile and may be labeled with erroneous lot numbers and expiry dates.

Product as listed by the FDA

Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright, Desire and See Clear.

Where it was distributed

Worldwide Distribution: US (nationwide) including states of: AZ, CA, DE, FL, GA, HI, LA, NJ, NY, NV, ON, PA and WA; and country of: Canada.

Nationwide Arizona California Delaware Florida Georgia Hawaii Louisiana New Jersey Nevada New York Pennsylvania Washington

Questions about this recall

Is Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition recalled?

Yes. The See Clear recalled Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition on 6 Jan 2017. The recall is Class II and its status is Ongoing. Recall number Z-1404-2017.

Why was it recalled?

Sterility and Misbranding: Lenses may not be sterile and may be labeled with erroneous lot numbers and expiry dates.

Which lots are affected?

All lots of lenses sold between 10/31/2013 to 10/31/2016

Where was it sold?

Worldwide Distribution: US (nationwide) including states of: AZ, CA, DE, FL, GA, HI, LA, NJ, NY, NV, ON, PA and WA; and country of: Canada.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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