Tag: fda_early_alert

FDA Issues Early Alert as Arrow International Removes Products With Spring Wire Guide Components

10 Nov 2026 3:39 p.m. · Source: US Food and Drug Administration

Arrow International, a Teleflex subsidiary, is removing products containing hydrophilic coated Spring Wire Guide components over a coating defect that could release particles into the bloodstream, the FDA says.

Health Business Science & Technology Medical Science Law Enforcement Social Issues Arrow International Teleflex Incorporated Spring Wire Guide FDA Early Alert Medical Device Recall Hydrophilic polymer emboli Product Recall Food Recalls FDA Drugs