FDA Medical Device Recalls (openFDA)
Kim's Trading Inc: Fancy i Color cosmetic lens, Contents: A pair of sterile soft color contact lens immersed in buffered isotonic saline solution, Size: B.C. 8.6mm DIA. 14.5mm. Dreamcon Co. LTD. Korea.
- Recall number
- Z-1756-2010
- Recalling firm
- Kim's Trading Inc
- Product
- Fancy i Color cosmetic lens, Contents: A pair of sterile soft color contact lens immersed in buffered isotonic saline solution, Size: B.C. 8.6mm DIA. 14.5mm. Dreamcon Co. LTD. Korea.
- Status
- Terminated
- Initiated
- 2010-05-17
- Posted
- 2010-06-04
- Terminated
- 2010-08-11
- Reason
- Recall is being conducted because the recalled color cosmetic contact lenses are unapproved medical devices.
- Root cause
- PMA
- Action
- Kim's Trading Inc. verbally contacted the distributor to provide notification of the recall. All affected product was to be properly disposed. For further information, contact Kim's Trading Inc. at 1-484-895-3773.
- Quantity
- 300 pairs of contact lens
- Distribution
- All product was distributed to one distributor in the Bethlehem PA area.
- Lot, serial or model codes
- Lot Number D01704: includes models Amber, Amethyst, Blueberry Crush, BumbleBee Yellow, Denim Blue, Envious Green, Honey, Pebble Gray, Marble Swirl, Royal Blue, Ultraviolet, HA11, HA12, HA13, HA14, HA16, HL21, HL22, HL23, HL24, HL26, Fierce Fandango and Holiday Green; Lot Number D01711: inlcudes models Copper, Gotham Gray, HJ31, HW21, HW22, Jade and Natural Hazel; Lot Number D01712: includes models Aquamist, Artic Blue, Deep Ocean Blue, HJ35, HJ36 and HW26; Lot Number D01713: includes models HJ33, HJ34, HW23, HW24, Lavender, Lazer Green, Sour Apple Green and Vibrant Violet; and Lot (unidentified): includes models 011, 015, 024, 029, 032, 033, 035, 043-1, 044, 046, 047, 049, 055, 063-1, 064, 071, 079, 085 and 088.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LPM
- Firm FEI
- 3008163473
- Firm city
- Bethlehem
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28