ASO recalls 10-count sterile gauze pads that may not be fully sterilized, posing a risk of infection. Consumers should check batch numbers and contact ASO for details.
Potential that gauze pads may not be fully sterilized
ASO is recalling 10-count sterile g: 3-inch x 3-inch gauze pads that may not be fully sterilized. This could lead to infection if used improperly.
The gauze pads may not be fully sterilized, which could lead to infection if used on cuts or wounds. This is a risk during normal use when the pads are applied to injured skin.
People who own or use these gauze pads for first aid. Those with open wounds or infections are at higher risk.
Check for the ASO item number 780655 and batch/lot number 2384-20180524 on the packaging. The product is sold in 10-count cardboard boxes.
Look for the ASO item number 780655 and batch/lot number 2384-20180524 on the packaging.
The recall states the gauze pads may not be fully sterilized, which could lead to infection. They are not recommended for use until the remedy is applied.
Check for the ASO item number 780655 and batch/lot number 2384-20180524 on the packaging. The product is sold in 10-count cardboard boxes.
The recall does not specify a remedy, so contact ASO directly for further instructions.
We’ve drafted a message you can send ASO to request your refund or repair — edit it as you like.
Subject: Recall Z-0525-2019 — ASO ASO Hello, I own a ASO that is covered by recall Z-0525-2019 from ASO. 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.
