CME America recalls BodyGuard Microset tubing (REF A120-003XYVA) due to potential under-delivery of fluids when used with infusion pumps. Affected units include specific lot numbers.
When using a specific tubing set with infusion pump system, may result in under deliver of fluids.
CME America is recalling BodyGuard Microset tubing sets that may cause under-delivery of fluids when used with infusion pumps. This could lead to inadequate medication or fluid delivery to patients.
The tubing set may not deliver fluids properly when connected to an infusion pump, potentially causing patients to receive less medication or fluids than intended. This could lead to inadequate treatment or complications.
Healthcare professionals using the BodyGuard Infusion Pump System with the recalled tubing sets are most at risk. Patients receiving intravenous treatments with these sets could experience under-delivery of fluids.
Check for the product code REF A120-003XYVA on the tubing set. The affected units include specific lot numbers listed in the recall notice.
Look for the lot numbers listed in the recall: 10636, 10653, 12117, 12836, 13156, 13279, 13656, 13978, 14057, 14188, 14545, 14790, 14966, 15073, 19486, 19490, 19492, 19834, 16173.
The product code is REF A120-003XYVA.
Affected lot numbers include 10636, 10653, 12117, 12836, 13156, 13279, 13656, 13978, 14057, 14188, 14545, 14790, 14966, 15073, 19486, 19490, 19492, 19834, 16173.
The tubing may cause under-delivery of fluids when used with infusion pumps, potentially leading to inadequate medication or fluid delivery to patients.
We’ve drafted a message you can send CME America to request your refund or repair — edit it as you like.
Subject: Recall Z-1442-2020 — CME America CME America Hello, I own a CME America that is covered by recall Z-1442-2020 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.
