KCI recalls V.A.C. Ulta Therapy Units with model CAPULTDEV01 and serial numbers GAAC06245-GAAC20993 due to potential system error alarms and inability to initiate therapy from broken occlusion sensors.
Due to potential system error alarm and the inability to initiate therapy as a result of broken occlusion sensors.
KCI is recalling specific V.A.C. Ulta Therapy Units that may have broken occlusion sensors, causing system error alarms and preventing therapy from starting. This could lead to ineffective wound treatment.
The device may have broken occlusion sensors that cause system error alarms and prevent therapy from initiating. This means the wound treatment may not work as intended.
Patients using the V.A.C. Ulta Therapy Unit for wound management are most at risk. The recall affects specific model numbers and serial numbers.
Check for model number CAPULTDEV01 and serial numbers listed in the recall (GAAC06245 to GAAC20993). The product is an integrated wound management system that provides negative pressure wound therapy.
Verify your model number (CAPULTDEV01) and serial number (GAAC06245-GAAC20993) to confirm if your device is affected.
The model number is CAPULTDEV01.
Serial numbers from GAAC06245 to GAAC20993 are affected.
The product may have broken occlusion sensors causing system error alarms and preventing therapy from initiating.
We’ve drafted a message you can send KCI to request your refund or repair — edit it as you like.
Subject: Recall Z-0507-2025 — KCI KCI Hello, I own a KCI that is covered by recall Z-0507-2025 from KCI. 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.
