Carefree Surgical Specialties recalls robotic laparoscopy gauze rolls due to potential contamination and incorrect gauze quantity in sterile packaging. Affected units may compromise sterility or cause incorrect dosing during surgery.
Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging
Carefree Surgical Specialties is recalling robotic and laparoscopy gauze rolls because they may contain biological contaminants that could compromise sterility, and the packaging might have the wrong amount of gauze. This could lead to infections or improper surgical procedures if used.
The gauze rolls could have biological foreign matter that might compromise sterility during surgery, increasing infection risk. Additionally, the packaging might contain an incorrect quantity of gauze, which could lead to improper dosing during procedures.
Surgical teams and hospitals using Carefree Surgical Specialties' robotic or laparoscopy gauze rolls are likely affected. Those performing surgeries with these products face the highest risk due to potential contamination.
Check for the model number 15505/25 on the packaging. The product is sold as 'Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS' and was manufactured with lot number 1645.
Verify the model number 15505/25 and lot number 1645 on the packaging to confirm if the product is affected.
The gauze rolls may contain biological foreign matter that could compromise sterility, and the packaging might have the wrong amount of gauze.
Look for the model number 15505/25 and lot number 1645 on the packaging.
The recall record does not specify a remedy, so contact Carefree Surgical Specialties directly for guidance.
We’ve drafted a message you can send Carefree Surgical Specialties to request your refund or repair — edit it as you like.
Subject: Recall Z-2282-2025 — Carefree Surgical Specialties Carefree Surgical Specialties Hello, I own a Carefree Surgical Specialties that is covered by recall Z-2282-2025 from Carefree Surgical Specialties. 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.
