Reported Jan 27, 2016 · Terminated
InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. Products are intended for…
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 CS Needleless IV Connector, Catalog Number RYM-7001. 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
- Catalog number RYM-7001 Lots
R01842R01889R01891and R01897Expire 03/2016
- Catalog number RYM-7001 Lots
- Amount recalled
- 46,600 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.
Want the full recall guide?
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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