Reported Feb 18, 2015 · Terminated
ARROW Epidural Needle Component (product number AN-05501). Epidural needles permit access to the epidural space and are…
Arrow International Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Arrow International Inc · 2400 Bernville Road · Reading, PA · 19605
Is this the product you have?
- ARROW Epidural Needle Component (product number AN-05501). Epidural needles permit access to the epidural space and are used as a conduit for epidural catheter placement.
- Lot codes and dates
- Product number AN-05501
- Lot numbers
23F13J0530RF2108954RF6127264RF8045530RF0021370RF3014600RF6127624RF8070744RF0035171RF3026989RF7031498RF8083748RF0050648RF5084669RF7043570RF8096949RF0075647RF5094931RF7088907RF8123534RF0092301RF5106225RF7090151RF9015869RF2021938RF5118327RF7102346RF9030002RF2044557RF5120725RF7113197RF9071402RF2058276RF6081852RF8018337RF9098526RF2083791RF6092570RF8020947and RF9113319
- Amount recalled
- 63022
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
The product labeling does not specify the 5 year shelf life of the product.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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