Recalls

Recall - Due to Presence of Undeclared Sildenafil

Recall - Due to Presence of Undeclared Tadalafil

Class I Recall - Due to Risk of False Results

Recall - Due to Microbial Contamination

Recall - Due to the Potential Presence of Visible Particulate

Recall - Due to Potential Contamination with Listeria Monocytogenes

Recall - Due to the Potential of Missing Labels on Some Pens

Class I Recall - Due to Cracked or Broken Suction System Power Switches

Recall - Due to Label-Mix Up

Class I Recall - Due to Early Failure of Backup Batteries that May Cause Unexpected Ventilator Shut Down

Class I Recall - Due to Battery Failure

Class I Recall - Due to Possible Obstructions That May Block Oxygen Flow to Patients

Recall - Due to the Presence of Undeclared Diclofenac and Dexamethasone

Recall - Due to Potential Microbial Contamination

Class I Recall - Due to Power Issue that May Cause Ventilator to Stop with or without Alarms

Recall - Due to Potential Hidden Drug Ingredients

Recall - Due to Possible Health Risk

Class I Recall - Due to Potential Balloon or Catheter Hub Separation That May Cause Patient Harm

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