FDA recall record

C.R. Bard Arctic Sun ArcticGel Pads - Medium, Product Code 317-07 recall — FDA Z-0590-2018

Label on product box contains the incorrect reference #317-09 while the shelf box label with barcode and the internal foil pouch label are correctly…

Class IIIclassification
Z-0590-2018official record ID
Dec 13, 2017report date

Recall record at a glance

Official recordZ-0590-2018
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmC.R. Bard, Inc.
Report dateDec 13, 2017
Recall initiation dateJun 2, 2017
Quantity128 units
LocationCovington, GA, United States

Official product description

Arctic Sun ArcticGel Pads - Medium, Product Code 317-07

Why the product was recalled

Label on product box contains the incorrect reference #317-09 while the shelf box label with barcode and the internal foil pouch label are correctly labeled with product code 317-07 and lot number NDAR0462.

Distribution information

Distributed domestically. Distributed internationally to Australia and Belgium.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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