DrugMay 31, 2017
DEXTROSE Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use recall — FDA D-0862-2017
Presence of Particulate Matter: human hair found within an internal sample syringe.
Class IFDA: OngoingHospira Inc.
Recall history in this database
Classification mix: Class II: 110, Class I: 31, Class III: 10.
Medical DeviceJan 18, 2017
Hospira Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended recall — FDA Z-1016-2017
Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Extension Set, 59 inch with Spin Lock Collar, Non-DEHP, identified above due to a confirmed customer report of an…
Class IIFDA: TerminatedHospira Inc.
DrugDec 14, 2016
Hospira 5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count recall — FDA D-0169-2017
Failed Stability Specifications: The recalled lots did not meet the specification for color and pH throughout shelf life.
Class IIIFDA: TerminatedHospira Inc.
Medical DeviceNov 16, 2016
Hospira Symbiq Two Channel Infuser recall — FDA Z-0362-2017
May go to a white screen due to a problem with the SOM2 module. A white screen is a diagnostic screen displayed to the user as part of the safety shutdown procedure of the device. The…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceNov 16, 2016
Hospira Symbiq One Channel Infuser recall — FDA Z-0361-2017
May go to a white screen due to a problem with the SOM2 module. A white screen is a diagnostic screen displayed to the user as part of the safety shutdown procedure of the device. The…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceNov 9, 2016
Hospira Symbiq Two Channel Infuser recall — FDA Z-0354-2017
Hospira has received reports of Malfunction S205 Backup Battery Failure alarms in Symbiq v3.13 pumps. This issue to an incorrect installation of components on some of the Power Supply…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceNov 9, 2016
Hospira Symbiq One Channel Infuser recall — FDA Z-0353-2017
Hospira has received reports of Malfunction S205 Backup Battery Failure alarms in Symbiq v3.13 pumps. This issue to an incorrect installation of components on some of the Power Supply…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceNov 2, 2016
Hospira Symbiq Two Channel Infuser recall — FDA Z-0306-2017
Symbiq Infusers have the potential to experience a white screen during titration of a Keep Vein Open (KVO) delivery. This can allow the clinician to select the "NEXT" button prior to…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceNov 2, 2016
Hospira Symbiq One Channel Infuser recall — FDA Z-0305-2017
Symbiq Infusers have the potential to experience a white screen during titration of a Keep Vein Open (KVO) delivery. This can allow the clinician to select the "NEXT" button prior to…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 28, 2016
Hospira LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number recall — FDA Z-2873-2016
Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 28, 2016
Hospira LifeCare PCA 3, PCA Serial List Number 12384 Allows for clinician administration or recall — FDA Z-2874-2016
Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this…
Class IIFDA: TerminatedHospira Inc.
DrugSep 21, 2016
Hospira DOBUTamine Injection, USP 250 mg/20 mL, 20 mL Vial, For IV Use Only, Must be Diluted recall — FDA D-1500-2016
Discoloration: Firm received complaints of product discoloration and particulates.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+3 Infusion Pump recall — FDA Z-2729-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+ Hyperbaric Infusion Pump recall — FDA Z-2722-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+ Infusion Pump recall — FDA Z-2723-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+ Infusion Pump with Hospira MedNet Software recall — FDA Z-2727-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+3 Infusion Pump with Hospira MedNet Software recall — FDA Z-2730-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+3 Infusion Pump recall — FDA Z-2725-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+ Infusion Pump recall — FDA Z-2724-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+3 Infusion Pump System recall — FDA Z-2728-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceSep 14, 2016
Hospira Plum A+ Infusion Pump with Hospira MedNet Software recall — FDA Z-2726-2016
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Class IIFDA: TerminatedHospira Inc.
Medical DeviceAug 24, 2016
Hospira RECEPTAL LINERS: 1L(1000mL), 1.5L (1500mL), 2L (2000mL) 1) List Number 43056-01 recall — FDA Z-2594-2016
Hospira has become aware of customers using the incorrect size Receptal liners with their Receptal canisters, e.g., 1.5 L liner, 2L liner or 3L liner with a 1L canister. It is possible that…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceAug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with recall — FDA Z-2593-2016
Hospira has become aware of customers using the incorrect size Receptal liners with their Receptal canisters, e.g., 1.5 L liner, 2L liner or 3L liner with a 1L canister. It is possible that…
Class IIFDA: TerminatedHospira Inc.
Medical DeviceJul 20, 2016
Hospira The LifeCare PCA Plus II infusion pump system is designed for safe, effective recall — FDA Z-2139-2016
Hospira has received reports of PCA pumps not detecting distal occlusions, one of which resulted in a serious injury. The issue is caused by normal wear and tear on the Half Nut (the…
Class IIFDA: TerminatedHospira Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Hospira, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.