Arrow recalls TheraCath Epidural Catheters with unsealed packaging that may compromise sterility. Affected units include specific lot numbers from 2013. Consumers should check their product details and contact Arrow for guidance.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling TheraCath Epidural Catheters with unsealed packaging that could lead to contamination. This risk affects medical devices used during epidural procedures, potentially causing infections if not properly sterilized.
The catheters may have unsealed packaging, which can compromise sterility. If the packaging is not properly sealed, the device might become contaminated during use, increasing infection risks during epidural procedures.
Healthcare professionals and patients who received TheraCath Epidural Catheters with the specified lot numbers. Those using the product for epidural anesthesia are most at risk.
Check the product label for lot numbers: 13F17B0147, 13F17C0176, 13F17C0419, 13F17E0464, 13F17F0039, 13F17F0498, 13F17F0609, 13F17F0789, 13F17G0250, 13F17J0076, 13F17K0413, 13F17K0414, 13F17K0415, 13F17K0416. The product was sold by Arrow International Inc. in 2013.
Look for the lot numbers listed in the recall notice to determine if your catheter is affected.
The catheter may have unsealed packaging, which can compromise sterility and increase infection risk during epidural procedures.
Check the product label for the specific lot numbers listed in the recall notice. If affected, contact Arrow International Inc. for further instructions.
The recall addresses potential contamination risk, but the official notice does not indicate a risk of serious injury or death.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2012-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2012-2018 from Arrow. 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.
