Reported Dec 30, 2020 · Completed
IceFORCE" 2.1 CX Cryoablation Needle
Boston Scientific 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: Boston Scientific Corporation · 1 Scimed Pl · Maple Grove, MN · 55311-1565
Is this the product you have?
- IceFORCE" 2.1 CX Cryoablation Needle
- Lot codes and dates
- UPNFPRPR3604
- UDIs
729010483102772901048310277290104831027729010483102772901048310277290104831027729010483102772901048310277290104831027729010483102772901048310277290104831027729010483102772901048310277290104831027
- Batch Numbers
U0903U0785U0617U0042T0166T0156A7083A6931A6928A6916A6734A1549A1527X1483A1203
- Amount recalled
- 75 units
This recall covers 37 products
The agency filed one notice per product. You are reading one of them; the other 36 are below.
24 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Complaint trend regarding needle shaft gas leaks.
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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