Abbott recalls FIRMap Catheter 60mm Basket models with incorrect labeling. This may cause confusion in medical use. Affected units have specific batch numbers and expiration dates.
Incorrect product labeling.
Abbott is recalling FIRMap Catheter 60mm Baskets due to incorrect product labeling. This could lead to confusion in medical use, potentially affecting patient safety.
Incorrect labeling could lead to confusion about the product's specifications. This might result in improper use or incorrect medical procedures if healthcare providers mistake it for another model.
Healthcare professionals using the catheter for medical procedures are most at risk. Patients receiving the catheter may also be affected if labeling causes errors.
Check for model number AR064060 and batch numbers listed: 2158303 (exp. 30 Nov 2022), 2159876 (exp. 31 Jan 2023), 2156510 (exp. 30 Sep 2022), 2162996 (exp. 31 Mar 2023), 2159875 (exp. 30 Nov 2022), or 2159877 (exp. 30 Nov 2022).
Look for model number AR064060 and batch numbers listed in the description.
Abbott recalls FIRMap Catheter 60mm Baskets due to incorrect product labeling.
Check the product label for model number AR064060 and batch numbers listed. If you have the affected batch numbers, contact Abbott for guidance.
The recall is for incorrect labeling, which could cause confusion in medical use but does not pose a direct risk of serious injury.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1213-2022 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1213-2022 from Abbott. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.