FDA recall record

Atrium 36Fr Right Angled Firm PVC Thoracic Catheter, (Pkg of 10) Part Number: 15236 recall — FDA Z-2346-2015

Inner pouches incorrectly labeled as part 8136, 36Fr Right Angled Thermosensitive PVC catheter, but are part 15236-36Fr Right Angled Firm PVC Catheter

Class IIclassification
Z-2346-2015official record ID
Aug 12, 2015report date

Recall record at a glance

Official recordZ-2346-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAtrium Medical Corporation
Report dateAug 12, 2015
Recall initiation dateJun 19, 2015
Quantity62 cases (10/cs)=620 units
LocationHudson, NH, United States

Official product description

Atrium 36Fr Right Angled Firm PVC Thoracic Catheter, (Pkg of 10) Part Number: 15236

Why the product was recalled

Inner pouches incorrectly labeled as part 8136, 36Fr Right Angled Thermosensitive PVC catheter, but are part 15236-36Fr Right Angled Firm PVC Catheter

Distribution information

AZ, CA, LA. IN, NC, TN, TX, VA

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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