Zoll recalls Quattro IV Premium Disposable Packs and Start Up Kits due to potential leaks from catheter or tubing. Affected units include all lots of model REF 870:8700-000766-01.
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Zoll is recalling its Quattro IV Premium Disposable Packs and Start Up Kits (6 ft.) because of potential leaks from the catheter or tubing. This could lead to contamination or infection risks if the leaks occur during medical use.
The recall addresses potential leaks from the catheter or the start-up kit tubing. If leaks happen during medical use, they could lead to contamination or infection risks for patients or healthcare workers.
Healthcare professionals using the Quattro IV system are most at risk, particularly those in settings where the device is used for critical patient care. Patients receiving treatment with this equipment may also be affected if leaks occur.
Check for the model number REF 8700-000766-01 on the Quattro IV Premium Disposable Pack and Start Up Kit (6 ft.). All lots of this product are affected.
Look for the model number REF 8700-000766-01 on the Quattro IV Premium Disposable Pack and Start Up Kit (6 ft.).
Yes, all lots of the Quattro IV Premium Disposable Pack and Start Up Kit (6 ft.) with model number REF 8700-000766-01 are affected.
Potential leaks from the catheter or tubing could lead to contamination or infection risks during medical use.
No specific action is required beyond checking the model number. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Zoll to request your refund or repair — edit it as you like.
Subject: Recall Z-0058-2022 — Zoll Zoll Hello, I own a Zoll that is covered by recall Z-0058-2022 from Zoll. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.