Smisson-Cartledge recalls ThermaCor 1200 disposable sets due to potential aluminum leaching into warmed fluids. Affected units include specific models and serial numbers sold for medical use.
Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.
Smisson-Cartledge is recalling ThermaCor 1200 disposable sets used in medical fluid infusion because aluminum ions might leach into warmed fluids. This could pose a risk to patients receiving these treatments.
The sets may release aluminum ions into warmed fluids, which could enter a patient's bloodstream during infusion. This poses a potential risk if aluminum levels become too high, though the exact impact is not specified in the recall.
Patients using ThermaCor 1200 sets for fluid infusion after surgery or trauma are affected. Healthcare providers using these sets for medical procedures are most at risk.
Check for model PNC-1200 or serial numbers on the sets. These are used in medical settings for fluid infusion after surgery or trauma.
Look for model PNC-1200 or serial numbers on the disposable sets used for medical fluid infusion.
The recall states potential aluminum ions leaching into warmed fluids, which could enter a patient's bloodstream during infusion.
The recall does not specify a stop-use instruction; the remedy is null, so users can continue using them but should check for the recalled model.
Check for model PNC-1200 or serial numbers on the disposable sets used for medical fluid infusion after surgery or trauma.
We’ve drafted a message you can send Smisson-Cartledge to request your refund or repair — edit it as you like.
Subject: Recall Z-1260-2021 — Smisson-Cartledge Smisson-Cartledge Hello, I own a Smisson-Cartledge that is covered by recall Z-1260-2021 from Smisson-Cartledge. 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.
