Recalls

Class I Recall - Due to Risk of Smoke or Fire When Lift Is Used with Depleted Battery

Class I Recall - Due to Potential Loose Catheter Marker Band That May Cause Patient Harm

Recall - Due to donor of the cornea tested reactive for HIV-1/HIV-2 Plus O antibody

Recall: Due to donor who tested reactive for HIV-1/HIV-2 Plus O antibody and HIV NAT

Recall - Due to Dissolution Test Failure

Class I Recall - Due to Distribution to U.S. Customers without Authorization, Clearance, or Approval from the FDA

Class I Recall - Risk of Misplaced Enteral Tubes Could Cause Patient Harm

Recall - Due to Microbial Contamination

Class I Recall - Due to Risk of False Positives Caused by Contamination