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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog number RYM-7001 Lots: R01842, R01889, R01891, and R01897, Expire 03/2016.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Rymed Technologies, LLC
- Reason for Recall:
- Potential for the female luer component of the InVision-Plus IV connector to crack during use.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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.
Product Codes/Lot Numbers:
Catalog number RYM-7001 Lots: R01842, R01889, R01891, and R01897, Expire 03/2016.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0676-2016
Related Recalls
Potential for the female luer component of the InVision-Plus IV connector to crack during use.