Arrow recalls TheraCath Epidural Catheters with incorrect expiration dates on labels, which may increase infection risk. Affected units have product code EC-050:13F18C0518.
The lidstock states the incorrect expiration date for the product. This issue could result in use of a device that is expired which could potentially lead to an increased risk of infection or other complications. Sterility, biocompatibility, safety, or efficacy of the kits and their components are not assured beyond the correct expiration date.
Arrow is recalling TheraCath Epidural Catheters that have incorrect expiration dates on their labels. Using these expired devices could increase the risk of infection or other complications during medical procedures.
The catheter label shows an incorrect expiration date. Using expired medical devices can compromise sterility and safety, potentially leading to infections or other complications during procedures.
Healthcare providers who use the Arrow TheraCath Epidural Catheter for medical procedures may be affected. Patients receiving epidural anesthesia are at risk if the catheter is used after the expiration date.
Check for product code EC-05000 with lot number 13F18C0518 on the label. The catheter is used for epidural space access in medical procedures.
Verify the expiration date on the catheter label matches the product code EC-05000 with lot number 13F18C0518.
The catheter label shows an incorrect expiration date, which could lead to using an expired device and increase infection risk.
Check the label for product code EC-05000 and lot number 13F18C0518. If the expiration date is incorrect, contact Arrow for guidance.
The recall states increased risk of infection or complications, but not serious injury in normal use. The danger level is low risk.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2803-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2803-2020 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.
