CME America recalls T34L syringe pumps with serial numbers starting 26294-70196 due to potential under infusion without alarm or pump damage from cleaning fluid. Affected users should check their serial numbers and contact CME America for details.
Multiple reasons: 1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated. 2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
CME America is recalling T34L syringe pumps that may cause under-infusion without alarms or damage from cleaning fluid. This could lead to incorrect medication delivery or pump failure during critical medical treatments.
The pump's motor block mechanism can wear out, causing under-infusion without triggering alarms. Cracks in the pump hardware may also be damaged by cleaning fluids, leading to potential pump failure during critical medical treatments.
Patients using the T34L syringe pump for continuous or intermittent medication delivery are most at risk. Healthcare providers and patients with specific medical conditions requiring precise fluid administration may be affected.
Check for serial numbers listed in the recall: 26294 to 70196. The product is used for continuous or intermittent medication delivery in clinical settings like hospitals or clinics.
Look for serial numbers starting with 26294 through 70196 on the pump's label.
Reach out to CME America for further instructions on how to handle the recalled pump.
The pump may have under-infusion without alarms due to motor block wear, or cracks that get damaged by cleaning fluids.
Check your serial number against the list provided and contact CME America for next steps.
The recall indicates potential risks, so it's recommended to check your serial number and contact CME America before using.
We’ve drafted a message you can send CME America to request your refund or repair — edit it as you like.
Subject: Recall Z-0525-2021 — CME America CME America Hello, I own a CME America that is covered by recall Z-0525-2021 from CME America. 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.
