Reported Jan 18, 2017 · Terminated
Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of…
Hospira 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: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP
- Latex-Free Intended useFor the administration of drugs and solutions to a patient's vascular system through a vascular access device
- Lot codes and dates
- Product List Number14699-28
- Lot Number17-077-NS
- Amount recalled
- 48,050 units
Where it was sold
- Nationwide
Why it was recalled
Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Extension Set, 59 inch with Spin Lock Collar, Non-DEHP, identified above due to a confirmed customer report of an occlusion of solvent in the male luer lock. This occlusion has the potential to prevent the set from being primed for use and cause a delay in therapy.
This product could cause temporary or reversible health problems — stop using it.
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