- Recalls.gov
- 0.9 Percent Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container by Baxter: Recall - Particulate Matter
- Lidocaine HCI Injection, USP, 2 percent, by Hospira: Recall: July 30, 2014
- Discontinue use of GenStrip Blood Glucose Test Strips by Shasta Technologies
- 1% Lidocaine HCI Injection, USP, by Hospira: Recall - Visible Particulates
- Teleflex Medical, ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port Urgent Recall
- Etomidate Injection/Pfizer-Mylan: Recall
- Lidocaine HCl Injection 2%, 5 ml Vial by Hospira: Recall - Presence of Particulate Matter
- Abrams Royal Pharmacy Sterile Products - Recall - Lack of Sterility Assurance
- Philips HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 Onsite Recall
- Meridian Medical Technologies Auto-Injectors: Extension of Expiration Dates
- Emergency Cricothyrotomy Kit By H&H Medical Corporation: Recall - Defective Cuff Balloon On Endotracheal Airway
- HeartSine Technologies Samaritan 300/300P PAD Public Access Defibrillators: Recall - Power, Battery Issues
- Metoclopramide Injection And Ondansetron Injection by Hospira: Recall - Glass Strand Particulates Caused By Glass Supplier