FDA recall record

C.R. Bard Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in recall — FDA Z-0198-2016

Incorrect unit labeling. The case label and shelf box are correct, Product Code 63512 and Catheter Size 12 French. The unit label (catheter package) may…

Class IIIclassification
Z-0198-2016official record ID
Nov 11, 2015report date

Recall record at a glance

Official recordZ-0198-2016
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmC.R. Bard, Inc.
Report dateNov 11, 2015
Recall initiation dateOct 2, 2015
Quantity4,170 each
LocationCovington, GA, United States

Official product description

Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in boxes of 30 units

Why the product was recalled

Incorrect unit labeling. The case label and shelf box are correct, Product Code 63512 and Catheter Size 12 French. The unit label (catheter package) may state Product Code 63516 and Catheter Size 16 French.

Distribution information

Nationwide Distribution including CA, FL, IL, MO, NJ, OR, PA, TX & WA.

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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