Hospira Inc.: 209 recalls on record

Recalls filed with 1 agency: FDA (209).

First recall on record: June 20, 2012. Most recent: May 31, 2017.

Risk classification: Class I: 53 · Class II: 147 · Class III: 9

Most recent recalls

DateAgencyProduct
September 18, 2013FDAPropofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), packaged in 5 Units x 20 mL Si…D-932-2013
September 4, 2013FDAKetorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 600…D-926-2013
September 4, 2013FDADiazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Via…D-927-2013
September 4, 2013FDA0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. La…D-922-2013
August 21, 2013FDAPropofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 mL, Single patient infusion …D-887-2013
August 14, 2013FDAOndansetron Injection, USP, 4mg/2mL, (2mg/ml), 2mL single-dose Fliptop Vial, Rx only, Ste…D-851-2013
August 14, 2013FDAList No. 14211-28; PLUM BLOOD SET; Prepierced Port, 200 Micron Filter, 110 Inch, Non-DEHP…Z-1855-2013
August 14, 2013FDAList No. 14207-28; BLOOD SET; 200 Micron Filter, 105 Inch, Non-DEHP; For Blood Product Ad…Z-1853-2013
August 14, 2013FDA0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., …D-836-2013
August 14, 2013FDAList No. 14203-28; BLOOD SET; 200 Micron Filter, 80 Inch, Non-DEHP; For Blood Product Adm…Z-1851-2013
August 14, 2013FDAList No. 14200-28; SECONDARY BLOOD SET; 200 Micron Filter, 36 Inch, Non-DEHP; For Blood P…Z-1850-2013
August 14, 2013FDAList No. 14217-28; Y-TYPE BLOOD SET; 200 Micron Filter, Prepierced Y-Site, Non-Vented, 80…Z-1857-2013
August 14, 2013FDAList No. 14206-28; Y-TYPE BLOOD SET; 200 Micron Filter, Cylinder Pump, Convertible Pin an…Z-1852-2013
August 14, 2013FDAList No. 14219-28; Y-TYPE BLOOD SET; 200 Micron Filter, Cylinder Pump, CLAVE Y-Site, Non-…Z-1858-2013
August 14, 2013FDAList No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Mic…Z-1854-2013
August 14, 2013FDAList No. 14212-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 …Z-1856-2013
August 7, 2013FDAThe Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, dru…Z-1847-2013
July 31, 2013FDASodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in…D-813-2013
July 24, 2013FDALifeShield; Sterile; Rx only; List No. 19666-28; SYMBIQ PUMP SET, CONVERTIBLE PIN, PIGGYB…Z-1751-2013
July 17, 2013FDAGentamicin Sulfate Injection USP 80 mg/2 mL(40 mg/mL as Gentamicin), 2 mL Single-dose Fli…D-686-2013
July 3, 2013FDA0.9% Sodium Chloride Irrigation, USP, 3000 mL, Rx Only, Hospira, Inc., Lake Forest, IL 60…D-617-2013
July 3, 2013FDA70% Dextrose Injection USP, 2000 mL, Rx Only, by Hospira, Inc., Lake Forest, IL 60045, ND…D-612-2013
July 3, 2013FDA0.9% Sodium Chloride Injection, USP, Polyolefin Flexible Container, a) 500 mL (NDC 0409-7…D-611-2013
July 3, 2013FDA20% Dextrose Injection, USP, a) 500 mL in 1000 mL Partial-Fill Container (NDC 0409-7935-1…D-616-2013
July 3, 2013FDA5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), by…D-614-2013

Questions about this company

How many recalls does Hospira Inc. have?
Recalert has 209 U.S. recalls on record for Hospira Inc., published between June 20, 2012 and May 31, 2017.
Which agencies have handled Hospira Inc. recalls?
Hospira Inc. appears as the recalling firm in recalls from: FDA (209).

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