FDA recall record

Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm, Product Code: AI-05210 recall — FDA Z-2068-2021

Marketed without a 510K

Class IIclassification
Z-2068-2021official record ID
Jul 21, 2021report date

Recall record at a glance

Official recordZ-2068-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmArrow International Inc.
Report dateJul 21, 2021
Recall initiation dateMay 19, 2021
Quantity48 units
LocationReading, PA, United States

Official product description

Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm, Product Code: AI-05210 - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.

Why the product was recalled

Marketed without a 510K

Distribution information

US Nationwide distribution in the states of FL, ID, IL, NY, OH, TX.

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

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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