Reported Jan 27, 2016 · Terminated
InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single…
Rymed Technologies, LLC
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: Rymed Technologies, LLC · 6000 W William Cannon Dr Ste B300 · Austin, TX · 78749-1991
Is this the product you have?
- InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Product as published RYM-5000InVision-Plus Lots 610, 611, 613, 614 RYM-5001Lots R01777, R01789, R01807, R01817, R01822, R01827, R01839, R01848, R01857, R01860, R01871, and R01874 RYM-8001Catalog number RYM-5001CL Lots R01825, R01887, and R01890. InVision Plus Junior Lot R01853. - Amount recalled
- 496,400 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Potential for the female luer component of the InVision-Plus IV connector to crack during use.
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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