Zoll recalls Solex 7 IV Disposable Packs and Start Up Kits due to potential leaks from catheter or tubing. Affected units include all lots of the product. No specific action is required per recall notice.
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Zoll is recalling Solex 7 IV Disposable Packs and Start Up Kits (6 ft.) because of potential leaks from the catheter or tubing. This could lead to contamination or infection if the leaks occur during use. The recall does not require immediate action as the hazard is not severe enough to cause serious injury.
The labeling update indicates that the catheter or start-up kit tubing might leak during use. Leaks could cause contamination or infection if the fluid leaks onto surfaces or clothing. However, the hazard is not described as causing serious injury or death.
Healthcare professionals using the Solex 7 IV system are most likely affected. Patients receiving IV treatments with this equipment could be at risk if leaks occur.
Check for the Solex 7 IV Disposable Pack and Start Up Kit (6 ft.) with the model number REF 870: 8700-000868-01. All lots of this product are affected.
Verify the product model number REF 8700-000868-01 on the Solex 7 IV Disposable Pack and Start Up Kit (6 ft.).
The recall does not require stopping use; the hazard is low risk and no specific action is needed.
Leaks could cause contamination or infection, but the hazard is not described as causing serious injury.
Check for the model number REF 8700-000868-01 on the Solex 7 IV Disposable Pack and Start Up Kit (6 ft.). All lots are affected.
We’ve drafted a message you can send Zoll to request your refund or repair — edit it as you like.
Subject: Recall Z-0062-2022 — Zoll Zoll Hello, I own a Zoll that is covered by recall Z-0062-2022 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.
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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.
