Angiodynamics Inc. (Navilyst Medical Inc.) recalls NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Ca
See all recalls from Angiodynamics Inc. (Navilyst Medical Inc.) →Recalled Product
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
Hazard / Issue
The product has the potential to be non-sterile as it was not packaged in accordance to specification.
Issued by
FDA
Affected States: CA, KY, MD, OR, VA, TX
Lot/Code Info: Lot Number: 5122528
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for NAMIC Fluid Delivery Set →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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