2014 Recalls and Alerts


10/16/14 - Hospira, Inc.
Hospira Announces Voluntary Nationwide Recall Of One Lot Of 1% Lidocaine HCI Injection, USP 10 MG Per ML, 30 ML Single-Dose. Preservative-Free, Due To Particulate Matter

10/14/14 - Hospira, Inc.
Hospira Announces Voluntary Nationwide Recall of Certain Lots of Several Lifecare Products Due to Potential for Leakage

10/10/14 - Covidien
Covidien Initiates Voluntary Field Safety Alert for Medi-Trace Cadence and Kendall Multi-Function Defibrillation Electrodes

9/11/14 - Hospira, Inc.
Hospira Issues a Voluntary Nationwide Recall of One Lot of Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), In 0.9% Sodium Chloride Injection, 500 mL, Due to Particulate Matter

8/8/14 - Cubist Pharmaceuticals Inc.
Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Nine Lots of CUBICIN (daptomycin for injection) 500 mg in 10 mL single use vials Following Complaints of Foreign Particulate Matter in Reconstituted Vials

8/6/14 - Cubist Pharmaceuticals Inc.
Cubist Pharmaceuticals Issues Voluntary U.S. Recall Of Certain Lots Of CUBICIN (Daptomycin For Injection) 500 mg In 10 mL Single Use Vials Due To Presence Of Particulate Matter

7/29/14 - Hospira, Inc.
Hospira Announces Voluntary Nationwide Recall Of One Lot Of Lidocaine HCI Injection, USP, 2 percent, 20 mg per mL Single-dose Vial, Preservative-free, Due To Particulate Matter

7/21/14 - American Health Packaging
American Health Packaging Announces the Voluntary Nationwide Recall of Ibuprofen Tablets, USP, 600 mg, 100 Hospital Unit Dose

7/21/14 - Unique Pharmaceuticals, Ltd.
Unique Pharmaceuticals Announces Voluntary Nationwide Recall of all Sterile Compounded Preparations Withing Their Expiry Period Due to a Lack of Sterility Assurance

7/14/14 - Baxter International, Inc.
Baxter Initiates Voluntary Worldwide Recall Of Four Lots Of IV Solutions Due To The Presence Of Particulate Matter

6/24/14 - Baxter International, Inc.
Baxter Initiates Voluntary Recall of One Lot of 0.9% Sodium Chloride Injection, USP Intravenous (IV) Solution

6/12/14 - Suncoast, Inc.
Diabetic Supply of Suncoast, Inc. issues a Nationwide Voluntary Recall of BMB-BA006A Advocate Redi-Code+ Blood Glucose Test Strips

5/21/14 - Fresenius Medical Care North America
Voluntary Nationwide and Canada Recall of NaturaLyte® Liquid Bicarbonate Concentrate Due to Potential Health Risk

5/16/14 - Hospira, Inc.
Hospira Announces Voluntary Nationwide Recall of One Lot of Labetalol Hydrochloride Injection, USP, 100 MG/10ML (5MG/ML), 20 ML, Multidose Vial, Due to Visable Particulates

5/16/14 - Ventlab LLC
Ventlab, LLC, Issues a Nationwide Recall of Ventlab Resuscitator Bags Due to Possible Health Risk

5/14/14 - NxStage Medical, Inc.
Voluntary Medical Device Recall, SAK Dialysate Concentrate, SAK-301, SAK-302, SAK-303, SAK 304, SAK 305, SAK 306, SAK 307, SAK 407

5/14/14 - Hospira, Inc.
Hospira Announces Voluntary Nationwide Recall of One Lot of Dobutamine Injection, USP, 250 MG, 20 ML, Single-Dose Fliptop Vial, Due To Visible Particulates

5/3/14 - CDC Health Advisory: Middle East Respiratory Syndrome Coronavirus (MERS-CoV)

4/29/14 - Shasta Technologies GenStrip
Shasta Technologies GenStrip Blood Glucose Test Strips May Report False Results

4/18/14 - Cubist Pharmaceuticals - CUBICIN
Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of One Lot of CUBICIN (daptomycin for injection) 500 mg in 10 mL single use vials Due to Presence of Particulate Matter

4/17/14 - Fresenius Medical Care North America
Fresenius Medical Care North American Voluntarily Recalls Certain Lots of NaturaLyte Bicarbonate Concentrate

3/18/2014 - Abbott Blood Glucose Monitor Recall
Abbott Issues Recall of Certain Blood Glucose Monitoring Systems

3/18/2014 - Hospira Hemostat Dual Channel Plum Set
Hospira Hemostat Dual Channel Plum Set: Recall-Risk of Over-Delivery of Blood Products

3/5/2014 - Baxter International, Inc.
Baxter Initiates U.S. Voluntary Recall of One Lot of Peritoneal Dialysis Solution Due to Container-Closure Non-Integrity

1/6/2014 - Fresenius
Fresenius 2008 Series Hemodialysis Machines, Class 2 Recall

1/2/2014 - Nipro Diagnostics, Inc.
Nipro Diagnostics, Inc. Initiates Voluntary Recall of Certain TRUEbalance and TRUEtrack Blood Glucose Meters

2013 FDA Recalls and Alerts