Cypress Medical recalls BinaxNOW Respiratory Strep A Test Kits due to shipping to customers without required licenses. No action needed as the issue is a licensing error, not a product defect.
Due to a classification error in our inventory management system, these medical devices were shipped to customers that did not have the requisite license to purchase such devices.
Cypress Medical is recalling BinaxNOW Respiratory Strep A Test Kits because they were shipped to customers who don't have the legal license to purchase these medical devices. This is a licensing error, not a product defect, so no action is required.
The test kits were shipped to customers who do not have the legal license to purchase them due to a classification error in the manufacturer's inventory system. This is a licensing issue, not a product defect.
Anyone who purchased the BinaxNOW Respiratory Strep A Test Kit (Catalog Number 730025) from a retailer. People without the required license to purchase medical devices are most at risk.
Check for the BinaxNOW Respiratory Strep A Test Kit with Catalog Number 730025. All lots are affected. The product has a GTIN of 10811877010453.
Verify if you have the required license to purchase medical devices from the manufacturer's website or your state health department.
No action is needed. This recall is due to a licensing error, not a product defect.
The manufacturer shipped the test kits to customers who do not have the legal license to purchase them due to an inventory management error.
No. This is a licensing issue, not a product defect. The test kits are safe to use if you have the required license.
We’ve drafted a message you can send Cypress Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-3184-2024 — Cypress Medical Cypress Medical Hello, I own a Cypress Medical that is covered by recall Z-3184-2024 from Cypress Medical. 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.
