Access Vascular recalls HydroMID 4Fr Single Lumen Basic Kit (Model 80004002) with incorrect expiration dates that could lead to expired catheters.
Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.
Access Vascular is recalling HydroMID 4Fr Single Lumen Basic Kit (Model 80004002) because some catheters in the kit have incorrect expiration dates. This could cause catheters to expire before the kit's labeled expiration date, potentially leading to unsafe use.
The catheters in certain lots have expiration dates that are earlier than the kit's labeled expiration date. This means the catheters could expire before the kit's expiration, potentially leading to unsafe use if the catheters are used after their actual expiration date.
Healthcare professionals using the HydroMID 4Fr Single Lumen Basic Kit (Model 80004002) are affected. Those who use the kit with catheters from specific lot numbers are most at risk.
Check for the model number 80004002 on the HydroMID 4Fr Single Lumen Basic Kit. Look for lot numbers 11428361, 11393260, or 11395226 on the catheters.
Verify the lot number on the kit matches 11428361, 11393260, or 11395226.
The recall is due to catheters in specific lots having expiration dates that expire before the kit's labeled expiration date.
Check the lot number on the kit. If it matches 11428361, 11393260, or 11395226, contact Access Vascular for instructions.
The risk is low as the issue involves expiration dates rather than immediate hazards like injury or malfunction.
We’ve drafted a message you can send Access Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-1129-2023 — Access Vascular Access Vascular Hello, I own a Access Vascular that is covered by recall Z-1129-2023 from Access Vascular. 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.
