Hospira Recalls
257 recalls on record · June 20, 2012 to May 31, 2017 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 14, 2013Medical DevicesFDA
Hospira Inc. recalls List No. 14212-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 Inch, Non-DEHP; For Blood Produ
Hazard: It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
August 14, 2013Medical DevicesFDA
Hospira Inc. recalls List No. 14211-28; PLUM BLOOD SET; Prepierced Port, 200 Micron Filter, 110 Inch, Non-DEHP; For Blood Product Administrat
Hazard: It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
August 14, 2013Medical DevicesFDA
Hospira Inc. recalls List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, No
Hazard: It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
August 14, 2013Medical DevicesFDA
Hospira Inc. recalls List No. 14207-28; BLOOD SET; 200 Micron Filter, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Ric
Hazard: It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
August 14, 2013Medical DevicesFDA
Hospira Inc. recalls List No. 14206-28; Y-TYPE BLOOD SET; 200 Micron Filter, Cylinder Pump, Convertible Pin and Non-Vented Pin, 80 Inch, Non-
Hazard: It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
August 14, 2013Medical DevicesFDA
Hospira Inc. recalls List No. 14203-28; BLOOD SET; 200 Micron Filter, 80 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica
Hazard: It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
August 14, 2013Medical DevicesFDA
Hospira Inc. recalls List No. 14200-28; SECONDARY BLOOD SET; 200 Micron Filter, 36 Inch, Non-DEHP; For Blood Product Administration; Made in
Hazard: It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
August 14, 2013DrugsFDA
Hospira, Inc. recalls Ondansetron Injection, USP, 4mg/2mL, (2mg/ml), 2mL single-dose Fliptop Vial, Rx only, Sterile, NDC 0409-4755-03, Hospira
Hazard: Presence of Particulate; lot being recalled as a precaution due to the discovery of 2 particles found in a lot which preceded the recalled lot
August 14, 2013DrugsFDA
Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409
Hazard: Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
August 7, 2013Medical DevicesFDA
Hospira Inc. recalls The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, elect
Hazard: The devices secondary audio signal fails to activate.
July 31, 2013DrugsFDA
Hospira Inc. recalls Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx o
Hazard: Presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plastic vial.
July 24, 2013Medical DevicesFDA
Hospira Inc. recalls LifeShield; Sterile; Rx only; List No. 19666-28; SYMBIQ PUMP SET, CONVERTIBLE PIN, PIGGYBACK, 2 CLAVES PORTS AND OPTION
Hazard: Hospira has received reports of customers experiencing air-in-line alarms related to administration sets that have a drip chamber with a ball valve. Preliminary investigation findings found that there is a potential for the ball valve to not seal the drip chamber as intended, leading to air in the line of the administration set.
July 17, 2013DrugsFDA
Hospira Inc. recalls Gentamicin Sulfate Injection USP 80 mg/2 mL(40 mg/mL as Gentamicin), 2 mL Single-dose Fliptop Vial, (NDC 0409-1207-13),
Hazard: Presence of Particulate Matter: visible particles were identified floating in the primary container.
July 3, 2013DrugsFDA
Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) 50 mL (NDC 0409-7984-36), c) 100 mL (0409-7984-37),
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 1.5% Glycine Irrigation, USP, 3000 mL, Rx Only, Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7974-08
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 0.9% Sodium Chloride Irrigation, USP, 3000 mL, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7972-08
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 20% Dextrose Injection, USP, a) 500 mL in 1000 mL Partial-Fill Container (NDC 0409-7935-19), b) 500 mL VisIV Container (
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), by Hospira, Inc., Lake Forest, IL
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 0.45% Sodium Chloride Injection, USP, Rx Only, 250 mL, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7132-02
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 70% Dextrose Injection USP, 2000 mL, Rx Only, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7120-07
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
July 3, 2013DrugsFDA
Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, Polyolefin Flexible Container, a) 500 mL (NDC 0409-7983-30), b) 1000 mL (NDC 0409-7
Hazard: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
June 26, 2013DrugsFDA
Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest,
Hazard: Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.
June 12, 2013DrugsFDA
Hospira Inc. recalls DOBUTamine in 5% Dextrose Injection, USP, 250 mg Total, 1000 mcg/mL 250 mL bag, Rx only, HOPIRA, INC., LAKE FOREST, IL 6
Hazard: Lack of Assurance of Sterility: Confirmed report of leaking in the primary container.
June 12, 2013DrugsFDA
Hospira Inc. recalls Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, ND
Hazard: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
May 15, 2013DrugsFDA
Hospira Inc. recalls Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL Single-Dose Fliptop, Rx only, HOSPIRA, INC. LAKE FOREST, IL
Hazard: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
May 15, 2013DrugsFDA
Hospira Inc. recalls QUELICIN (succinylcholine chloride) Injection, USP, 200 mg (20 mg/mL) 10 mL, Rx only, HOSPIRA, INC. LAKE FOREST, IL 6004
Hazard: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
May 15, 2013DrugsFDA
Hospira Inc. recalls Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA
Hazard: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
May 15, 2013DrugsFDA
Hospira Inc. recalls Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, ND
Hazard: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
May 8, 2013Medical DevicesFDA
Hospira Inc. recalls The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospita
Hazard: Pump shutting off during use without warning.