Rymed Technologies, Inc. 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Rymed Technologies, Inc.
Lot Codes / Batch Numbers
Lots #500, 502, 503, 504 and 505.
Products Sold
Lots #500, 502, 503, 504 and 505.
Rymed Technologies, Inc. is recalling RYM-5001 InVision-Plus Neutral Displacement I.V. Connector, packaged 100 units per box, 5 boxes per due to Weld failures on IV connector (area of female luer and spike body). Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Weld failures on IV connector (area of female luer and spike body)
Recommended Action
Per FDA guidance
Consignees were notified by e-mail and/or phone on 05/25/06 regarding the recall. Distributors were asked to return product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026