RYM-5001 InVision-Plus Neutral Displacement I.V. Connector, packaged 100 units per box, 5 boxes per case (500 units/case); labeled as Sterile-Nonpyrogenic; assembled in Mexico for Rymed Technologies, Inc., Austin, TX.
This recall has been terminated (originally issued December 30, 2006).
- Company
- Rymed Technologies, Inc.
- Recall Initiated
- May 25, 2006
- Posted
- December 30, 2006
- Terminated
- March 26, 2007
- Recall Number
- Z-0321-2007
- Quantity
- 28,479 units.
- Firm Location
- Austin, TX
- Official Source
- View on FDA website ↗
Reason for Recall
Weld failures on IV connector (area of female luer and spike body)
Distribution
Nationwide Recall
Lot / Code Info
Lots #500, 502, 503, 504 and 505.
Root Cause
Other
Action Taken
Consignees were notified by e-mail and/or phone on 05/25/06 regarding the recall. Distributors were asked to return product.