Reported Nov 6, 2019 · Terminated
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Centurion Medical Products Corporation
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: Centurion Medical Products Corporation · 100 Centurion Way · Williamston, MI · 48895-9086
Is this the product you have?
- PORT ACCESS INFUSION KIT - 1"
- NEEDLE Product CodeDYNDC2817
- Lot codes and dates
- Lot Number Expiration 2019060390 11/30/2020
- Amount recalled
- 200 kits
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Supplier initiated recall of the GRIPPER Needles
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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