Banner University Med Ctr recalls Cardiac Cath Lab Pack-170278 (GSCC40G) due to potential sterility issues with procedure trays. Affected units may not meet sterility standards for medical procedures.
Sterility assurance with procedure trays
American Contract Systems Inc. recalls Banner University Med Ctr's Cardiac Cath Lab Pack-170278 (model GSCC40G) because procedure trays may not maintain sterility. This could lead to infections during medical procedures if used improperly.
The procedure trays in this kit may not maintain sterility during medical procedures. If contaminated, they could lead to infections in patients during cardiac catheterization. This risk is specific to the trays' handling and storage.
Healthcare professionals using this cardiac catheterization lab kit in medical facilities are most at risk. Patients undergoing procedures with this kit could be affected if sterility is compromised.
Check for the model number GSCC40G on the product label. The kit was sold with lot code 9219618 and expires January 21, 2026. This recall applies to medical facilities using the Banner University Med Ctr Cardiac Cath Lab Pack.
Look for the model number GSCC40G on the product label to confirm if it's affected.
The recall indicates potential sterility issues with procedure trays, so it's not recommended for use until the remedy is applied. However, the specific remedy is not stated in the recall record.
Check for the model number GSCC40G on the product label. The kit was sold with lot code 9219618 and expires January 21, 2026.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected model.
We’ve drafted a message you can send Banner University Med Ctr to request your refund or repair — edit it as you like.
Subject: Recall Z-1426-2025 — Banner University Med Ctr Banner University Med Ctr Hello, I own a Banner University Med Ctr that is covered by recall Z-1426-2025 from Banner University Med Ctr. 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.
