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FDA Medical Device Recalls (openFDA)

K C Pharmaceuticals Inc: Sterile Multi-Purpose Solution, NO RUB, for soft hydrophylic contact lenses. 12 fl oz. bottles. Sold under the following brand names: Family Dollar HomeBest HEB Meijer Food Lion health PRIDE Stop and Shop Super G sunmark Brite-Life Wegmans Our Family Healthy Generations GoodSense Winn Dixie Finast Western Family K C Pharmaceuticals

Recall number
Z-0060-05
Recalling firm
K C Pharmaceuticals Inc
Product
Sterile Multi-Purpose Solution, NO RUB, for soft hydrophylic contact lenses. 12 fl oz. bottles. Sold under the following brand names: Family Dollar HomeBest HEB Meijer Food Lion health PRIDE Stop and Shop Super G sunmark Brite-Life Wegmans Our Family Healthy Generations GoodSense Winn Dixie Finast Western Family K C Pharmaceuticals
Status
Terminated
Initiated
2004-10-04
Posted
2004-10-28
Terminated
2011-11-01
Reason
Routine testing indicates product does not meet the expiration date in all cases.
Root cause
Other
Action
Product is being recalled due to concern that the product does not meet it's expiration date. Firm sent letters to it customers requesting them to remove product from stores and to destroy it. A destruction form was sent with a request to mail it back.
Quantity
2,252,664
Distribution
Nationwide
Lot, serial or model codes
All Codes
510(k) numbers
not on file
PMA numbers
not on file
Product code
LPN
Firm FEI
2026940
Firm city
Pomona
Firm state
CA
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

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