Z-0060-05

Sterile Multi-Purpose Solution, NO RUB, for soft hydrophylic contact lenses. 12 fl oz. bottles. Sold under...

Name: Z-0060-05 Sterile Multi-Purpose Solution, NO RUB, for soft hydrophylic contact lenses. 12 fl oz. bottles. Sold under...
Creator: K C Pharmaceuticals Inc
Published: 2004-10-04
License: https://open.fda.gov/license/

K C Pharmaceuticals Inc / initiated 2004-10-04 / Terminated

FDA source

K C Pharmaceuticals Inc began a recall of Sterile Multi-Purpose Solution, NO RUB, for soft hydrophylic contact lenses. 12 fl oz. bottles. Sold under the following brand names: Family Dollar HomeBest... on 2004-10-04. The reason FDA records is "Routine testing indicates product does not meet the expiration date in all cases". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0060-05
Status: Terminated
Initiated: 2004-10-04
Posted: 2004-10-28
Terminated: 2011-11-01
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
Product code: LPN Accessories, Soft Lens Products
Reason for recall: Routine testing indicates product does not meet the expiration date in all cases.
FDA 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 in commerce: 2,252,664
Distribution: Nationwide
Product codes and lots: All Codes

Product code LPN

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)