FDA recall record

C.L.R. Medicals International Viscocel and Viscocel Plus recall — FDA Z-0531-2014

CLR Medicals International Inc., initiated a nationwide recall of Viscocel and Viscocel Plus, in response to FDA inspection findings of deficiencies in…

Class Iclassification
Z-0531-2014official record ID
Jan 1, 2014report date

Recall record at a glance

Official recordZ-0531-2014
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmC.L.R. Medicals International, Inc.
Report dateJan 1, 2014
Recall initiation dateNov 25, 2013
Quantity249,592 units
LocationPomona, CA, United States

Official product description

Viscocel and Viscocel Plus. These products are intraocular fluid devices consisting of non-gaseous fluid intended to be introduced into the eye to aid performance of surgery, such as to maintain anterior chamber depth, preserve tissue integrity, protect tissue from surgical trauma, or function as a tamponade during retinal reattachment.

Why the product was recalled

CLR Medicals International Inc., initiated a nationwide recall of Viscocel and Viscocel Plus, in response to FDA inspection findings of deficiencies in the Quality System Regulations for Medical Device Manufacturers, 21 Code of Federal Regulation (CFR) Part 820 and lack of Premarket Approval (PMA) for devices sold or distributed in domestic commerce. The Viscoelastic products, intended for human

Distribution information

Worldwide Distribution - USA (nationwide) and Internationally to Egypt, Mexico, and Canada.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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