Arrow Endurance Extended Dwell Catheter Recall: Sterility Risk in Specific Lots
Arrow recalls specific lots of Endurance Extended Dwell Peripheral Catheters due to potential sterility issues. Affected units may not be sterile, risking infection during medical procedures.
Lower-risk recall
Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.
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What happened, in plain English
Arrow is recalling specific lots of Endurance Extended Dwell Peripheral Catheters because they may not be sterile, which could lead to infections during medical procedures. Patients using these catheters should contact Arrow for details. Read more at govinfonow.com/recall/66399-arrow-endurance-extended-dwell-catheter-recall-sterility-risk-in-specific.
Source Summary by GovInfoNow · govinfonow.com/recall/66399-arrow-endurance-extended-dwell-catheter-recall-sterility-risk-in-specific · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0837-2020
Cite this page
“Arrow Endurance Extended Dwell Catheter Recall: Sterility Risk in Specific Lots.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66399-arrow-endurance-extended-dwell-catheter-recall-sterility-risk-in-specific. Based on FDA recall #Z-0837-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0837-2020%22&limit=1).
Why it’s dangerous
The catheters in specific manufacturing lots may not be sterile, which could lead to infections if used during medical procedures. This is a potential sterility issue that could compromise patient safety.
Who’s affected
Patients using the recalled catheters for medical procedures are affected. Healthcare providers who use these specific lots for treatments are at risk of potential infection.
How to tell if you have this one
Check for the product code ASK-00820-FLH and manufacturing lots 13F19E0247, 13F19F0006, or 13F19G0433. The catheters were sold with expiration dates from August to September 2020.
- Brand
Arrow- Category
Medical device
What to do — step by step
Check Product Details
Identify the product code ASK-00820-FLH and manufacturing lots 13F19E0247, 13F19F0006, or 13F19G0433 to confirm if your catheter is affected.
Where it went and when
Where it was distributed
Distributed in Florida.
FDA distribution: “US: FL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida.
Recall timeline
FDA terminated this recall 23 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have the recalled catheter?
Contact Arrow directly to check if your catheter is affected and follow their instructions.
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Where this comes from
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.
- Official source: FDA Recall #Z-0837-2020 (December 6, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0837-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.