Centurion Cath Kit (Catalog #CKF105L) recalled due to temperature excursions from June to August 2021 potentially reducing effectiveness. Affected units sold between June 1 and September 30, 2021.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Centurion Cath Kit (Catalog #CKF105L) is recalled because it may have been exposed to higher temperatures during shipping from June to August 2021, which could reduce its effectiveness. This means the product might not work as intended for medical use.
The catheter kit was exposed to higher temperatures during shipping from June to August 2021, which could have reduced its effectiveness. This means the product might not work as intended for medical procedures.
Healthcare facilities that purchased this catheter kit between June 1 and September 30, 2021, are most at risk. Patients using the kit may experience reduced effectiveness if the product was affected by temperature issues.
Check for the catalog number CKF105L on the kit. The product was sold between June 1 and September 30, 2021, and may have been affected by temperature excursions during shipping.
Look for the catalog number CKF105L on the kit to confirm if it was affected by temperature excursions.
The catheter kit was exposed to higher temperatures during shipping from June to August 2021, which could have reduced its effectiveness.
The affected units were sold between June 1 and September 30, 2021.
Check the catalog number CKF105L on the kit to see if it was affected by temperature excursions. No specific action is required if it's not affected.
We’ve drafted a message you can send Centurion to request your refund or repair — edit it as you like.
Subject: Recall Z-1630-2022 — Centurion Centurion Hello, I own a Centurion that is covered by recall Z-1630-2022 from Centurion. 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.
