FDA recall record

Churchill Medical Systems Bifurcated set with check vales and Bionectors, Product Code recall — FDA Z-1476-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIclassification
Z-1476-2015official record ID
Apr 29, 2015report date

Recall record at a glance

Official recordZ-1476-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmChurchill Medical Systems, Inc.
Report dateApr 29, 2015
Recall initiation dateJan 15, 2015
Quantity1050
LocationDover, NH, United States

Official product description

Bifurcated set with check vales and Bionectors, Product Code: BN-2082CV Accessory device used to administer medical fluids

Why the product was recalled

Potential for leaking caused by insufficient bond between needleless device and female luer.

Distribution information

Nationwide Distribution including TX, OH, NY, CA, UT, PA, MA, NY, VA, and IL.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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

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