Reported Jun 8, 2022 · Terminated

FIRMap" Catheter, 60mm Basket

Abbott

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Abbott · 5050 Nathan Ln N · Plymouth, MN · 55442-3209

Is this the product you have?

  • FIRMap" Catheter, 60mm Basket
Lot codes and dates
  • Model NumberAR064060
  • UDI Number( 01) 0 0810591 02002 4 ( 17) 020531 ( 00) 1 2345678 95
  • Batch Numbers2158303 (Exp
  • Date
    • 30 NOV 2022)
    • 2159876 (Exp
  • Date
    • 31 JAN 2023)
    • 2156510 (Exp
  • Date
    • 30 SEP 2022)
    • 2162996 (Exp
  • Date
    • 31 MAR 2023)
    • 2159875 (Exp
  • Date
    • 30 NOV 2022)
    • and 2159877 ( Exp
  • Date30 NOV 2022)
Amount recalled
40 units

Where it was sold

Why it was recalled

Incorrect product labeling.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 18, 2024 · Data as of Sep 19, 5:42 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.