Arrow recalls NextStep Retrograde Replacement Hub Set due to incorrect expiration date on product, which may lead to infection risks if used after expiration.
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 NextStep Retrograde Replacement Hub Sets because the expiration date on the product label is incorrect. Using expired medical devices can increase the risk of infection or complications.
The product has an incorrect expiration date on its label. Using expired medical devices can lead to increased infection risks or complications because the sterility and safety of the device may be compromised.
Patients using this hub set for medical procedures may be affected if the product is expired. Healthcare providers who use these sets are most at risk of potential infection complications.
Check for product code NRH-15192 and lot number 13F19H0454 on the hub set. This product was sold by Arrow International Inc.
Verify the expiration date on the product label to ensure it is correct.
The product has an incorrect expiration date on its label, which could lead to increased infection risks if used after expiration.
The recall does not specify a remedy, so check the expiration date and contact Arrow International Inc. for further instructions.
The recall states potential infection risks, but no serious injury mechanism is described, so the risk is low.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2804-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2804-2020 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.
