Galt Medical recalls Introducer Kit- Tearaway MicroSlide with potential open seal in sterile packaging. Affected units include specific model numbers and lot numbers. Consumers should check their product details and contact the company for guidance.
Due to a potential open seal in the sterile barrier packaging.
Galt Medical is recalling certain Introducer Kit- Tearaway MicroSlide products due to a potential open seal in the sterile packaging. This could lead to contamination risks during medical procedures, making it important for healthcare providers to stop using these kits immediately.
The sterile packaging may have an open seal, which could allow contamination during medical procedures. This poses a risk of infection or improper device function if the packaging is not properly sealed.
Healthcare providers using these kits for medical procedures are most at risk. Patients receiving procedures with these kits may also be affected if the packaging is compromised.
Check for model numbers KIT-051-01, INT-101-15, and lot numbers 24298473, 24190504, 24284447 on the packaging. These kits are used for introducing catheters into blood vessels during medical procedures.
Look for model numbers KIT-051-01, INT-101-15 and lot numbers 24298473, 24190504, 24284447 on the packaging.
The recall is due to a potential open seal in the sterile packaging, which could lead to contamination during medical procedures.
Check the product details to see if it matches the recalled model numbers and lot numbers. Contact Galt Medical for further guidance.
The recall record does not mention a specific remedy or fix for this issue.
We’ve drafted a message you can send Galt Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1737-2025 — Galt Medical Galt Medical Hello, I own a Galt Medical that is covered by recall Z-1737-2025 from Galt Medical. 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.
