Reported Feb 17, 2021 · Terminated
Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, Neutral Fluid…
Baxter Healthcare 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: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, Neutral Fluid Displacement, 5.7 " (14 cm)
- REF 7N8370K - Product Usageintended for single patient use with a vascular access device for the administration of drugs and solutions without needles, thus eliminating the potential for needle-stick injuries during use
- Lot codes and dates
- UDI00085412613505
- Lot Numbers
DR18E01023exp. 5/2/2023DR18E07053exp. 5/8/2023DR19G08023exp. 7/8/2024DR19H07015exp. 8/7/2024DR19L09030exp. 12/10/2024DR20B04020exp. 2/5/2025
- Amount recalled
- 66,800 units
Where it was sold
Why it was recalled
There were customer reports of separation between the tubing and Male Luer Lock Adaptor.
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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