FDAFDA · Food and drugs·Recall number Z-0675-2016
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.
Published January 27, 2016 · Recall initiated: January 5, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential for the female luer component of the InVision-Plus IV connector to crack during use.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Rymed Technologies, LLC
- Distributor
- US Nationwide Distribution.
- Lot
- InVision-Plus Catalog number RYM-5000 Lots 610, 611, 613, 614; Catalog number RYM-5001 Lots R01777, R01789, R01807, R01817, R01822, R01827, R01839, R01848, R01857, R01860, R01871, and R01874; Catalog number RYM-5001CL Lots R01825, R01887, and R01890. InVision Plus Junior Catalog number RYM-8001 Lot R01853.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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