Reported Dec 5, 2018 · Terminated
Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA06100 Product Usage: Recommended for use in catheterization…
Numed 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: Numed Inc · 2880 Main Street /Rt 11b · Hopkinton, NY · 12965
Is this the product you have?
- Multi-Track Angiographic
- Catheter (MMTA) Product CodeMMTA06100
- Product UsageRecommended for use in catheterization for angiography of cardiovascular vessels and I or chambers. It can be used for injection of contrast medium and pressure measurement in any chamber or vessel
- Lot codes and dates
- Lot numbers
6MT-06456MT-0646 Exp
- Date2023-09-30
- UDI04046964312861
- Lot numbers
- Amount recalled
- 100 units
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
Why it was recalled
Instructions for Use booklets were not included on the outer pouch
This product could cause temporary or reversible health problems — stop using it.
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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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