CLASS II ONGOING Device recall · Reported 5 Aug 2020 · FDA Enforcement Report
Ttdeye (brand) Flower Brown, B16112210 recalled
Chengdu Ai Qin E-commerce is recalling Ttdeye (brand) Flower Brown, B16112210, distributed nationwide in the US. The recall was initiated on 23 Jun 2020 and the FDA has classified it as Class II.
Check your package
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-2710-2020
- FDA event ID
- 85923
- Recalling firm
- Chengdu Ai Qin E-commerce, Gao Xin, N/A
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 23 Jun 2020
- FDA classified
- 27 Jul 2020
- Reported
- 5 Aug 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Other Reasons
- Device type
- Contact Lenses & Eye Devices
Timeline
| 23 Jun 2020 | Recall initiated by company | |
| 27 Jul 2020 | Classified by FDA | +34 days |
| 5 Aug 2020 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Colored contact lenses were distributed without FDA clearance.
Product as listed by the FDA
TTDEYE (brand) Flower Brown, B16112210 - Product Usage: Colored contact lenses
Where it was distributed
US Nationwide distribution.
Stores named: Online Retailers
Questions about this recall
Why was it recalled?
Colored contact lenses were distributed without FDA clearance.
Which lots are affected?
Date of manufacture: 2018-08
Where was it sold?
US Nationwide distribution.
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
6 other products · FDA event 85923This product is part of a recall event; the main page for the event is Ttdeye (brand) Radial Brown, B16112109 recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Ttdeye (brand) Radial Brown, B16112109 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide | |
| CLASS II | Ttdeye (brand) Radial Pink, B16112110 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide | |
| CLASS II | Ttdeye (brand) Black Starshine, B16112100 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide | |
| CLASS II | Ttdeye (brand) Devil Red, B16112201 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide | |
| CLASS II | Ttdeye (brand) Diamonds Starlight, B16112203 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide | |
| CLASS II | Ttdeye (brand) Flower Grey, B16112231 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide |
More recalls from Chengdu Ai Qin E-commerce
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Ttdeye (brand) Flower Grey, B16112231 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide |
| Device | CLASS II | Ttdeye (brand) Diamonds Starlight, B16112203 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide |
| Device | CLASS II | Ttdeye (brand) Devil Red, B16112201 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide |
| Device | CLASS II | Ttdeye (brand) Black Starshine, B16112100 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide |
| Device | CLASS II | Ttdeye (brand) Radial Pink, B16112110 recalled | Chengdu Ai Qin E-commerce | Other | Nationwide |
Other Contact Lenses & Eye Devices recalls
All 152| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Tecnis Eyhance Iol with Tecnis Simplicity" Delivery System recalled | AMO Puerto Rico Manufacturing | Device Malfunction | Nationwide |
| Device | CLASS II | Alcon PRECISION1 One-Day Contact Lenses, -2.25D recalled | Alcon Research | Sterility | 19 states |
| Device | CLASS II | Sofmed Breathables, (stenfilcon A) contact lens recalled by CooperVision | CooperVision | Sterility | Nationwide |
| Device | CLASS II | Voyant 1-Day Premium Toric, (stenfilcon A) contact lens recalled | CooperVision | Sterility | Nationwide |
| Device | CLASS II | MyDay Toric, stenfilcon A) Contact Lens recalled by CooperVision | CooperVision | Sterility | Nationwide |