Hospira recalls

Hospira has 225 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 31 May 2017. 10 are still ongoing. The most frequent reason is sterility.

Total recalls225since 2012
Last 12 months0reported
Class I6027% of total
Ongoing10latest 31 May 2017

Recalls per month, last 24 months

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Severity split

Class I 60 27%Class II 153 68%Class III 12 5%

By year

Ongoing hospira recalls

10 active

All hospira recalls, newest first

225 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IInfant 25% Dextrose Injection recalled by HospiraDextroseHospiraParticulate MatterNationwide
DeviceCLASS IIMinibore Extension Set with Spin Lock Collar, Non-DEHP, Latex-Free recalledHospiraOtherNationwide
DrugCLASS III5% Lidocaine HCL and 7.5% Dextrose Injection, USP Single-dose ampule recalledHospiraPotency & AssayPR
DrugCLASS IIFentanyl Citrate Injection, USP, 100 mcg Fentanyl recalled by HospiraHospiraSterilityNationwide
DeviceCLASS IILifeCare PCA 3, PCA recalled by HospiraHospiraDevice MalfunctionNationwide
DrugCLASS IIDOBUTamine Injection, USP 250 mg/ Vial, For IV Use Only recalledHospiraParticulate MatterNationwide
DeviceCLASS IIPlum A+3 Infusion Pump System recalled by HospiraHospiraDevice MalfunctionNationwide
DeviceCLASS IIPlum A+ Infusion Pump recalled by HospiraHospiraDevice MalfunctionNationwide
DeviceCLASS IIPlum A+ Hyperbaric Infusion Pump recalled by HospiraHospiraDevice MalfunctionNationwide
DeviceCLASS IIReceptal Canisters: Canister, Ats recalled by HospiraHospiraDevice MalfunctionNationwide
DeviceCLASS IIReceptal Liners: List Number recalled by HospiraHospiraDevice MalfunctionNationwide
DeviceCLASS IIThe LifeCare Pump recalled by HospiraHospiraDevice MalfunctionNationwide
DrugCLASS IIDiazepam Injection USP 10mg/ (5 mg/mL recalled by HospiraDiazepamHospiraParticulate MatterNationwide
DrugCLASS IMagnesium Sulfate Inj., USP 50%/mL) recalled by HospiraHospiraParticulate MatterNationwide
DeviceCLASS II*** Product labeled in part: List No. recalled by HospiraHospiraPackaging DefectsNationwide
DeviceCLASS II*** Product labeled in part recalled by HospiraHospiraPackaging DefectsNationwide
DeviceCLASS II*** Product labeled in part: List No. recalled by HospiraHospiraPackaging DefectsNationwide
DeviceCLASS II*** Product labeled in part recalled by HospiraHospiraPackaging DefectsNationwide
DeviceCLASS II*** Product labeled in part recalled by HospiraHospiraPackaging DefectsNationwide
DrugCLASS IIVancomycin Hydrochloride for Injection, USP vial recalled by HospiraHospiraParticulate MatterNationwide
DeviceCLASS IIThe Plum 360 is a large volume infuser capable recalled by HospiraHospiraForeign MaterialIL
DeviceCLASS IIThe Plum A+ is a dual-line volumetric infusion system recalledHospiraForeign MaterialIL
DrugCLASS I8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL) (84 mg/mL) recalledHospiraParticulate MatterNationwide
DrugCLASS IIIMagnesium Sulfate Inj., USP 50%/mL) recalled by HospiraHospiraPotency & AssayNationwide
DrugCLASS IIIQuelicin (Succinylcholine Chloride) Injection, USP 200 mg. recalledQuelicinHospiraForeign MaterialNationwide
DrugCLASS IIAminosyn-PF (amino acids) 7%, Sulfite-Free recalled by HospiraHospiraUndeclared SulfitesNationwide
DrugCLASS IIPotassium Chloride Injection 20 mEq, 400 mEq/L recalled by HospiraHospiraPackaging DefectsNationwide
DrugCLASS IIDextrose Injection, USP, 70%, Packaged as recalled by HospiraHospiraPackaging DefectsNationwide
DrugCLASS IIDextrose Injection, USP, 50%, Packaged as recalled by HospiraHospiraPackaging DefectsNationwide
DrugCLASS IIMannitol I.V. recalled by HospiraHospiraPackaging DefectsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.