InVision-Plus CS Needleless IV Connector recall
InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. Products are intended for single patient use in intravenous…
Why was InVision-Plus CS Needleless IV Connector recalled?
Potential for the female luer component of the InVision-Plus IV connector to crack during use.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Catalog number RYM-7001 Lots: R01842, R01889, R01891, and R01897, Expire 03/2016.
- Product
- InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. Products are intended for single patient use in intravenous…
- Recalling firm
- Rymed Technologies, LLC
- Quantity
- 46,600 units
- Distribution
- US Nationwide Distribution.
- Recall date
- January 27, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)