Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 2822128240 of 50,591 recalls

Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Medline 300-350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿ Recalled by...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Intermed 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ ¿¿¿ Recalled...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex Unit Dose 5 ml Normal Saline (0.9%)¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Medline Prefilled 550 ml Sterile¿¿ ¿ Recalled by Medex Cardio-Pulmonary...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Intermed 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex Unit Dose 15 ml Normal Saline ¿ Recalled by Medex Cardio-Pulmonary...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿¿ ¿¿¿ ¿¿¿...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 1000 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ Recalled by...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 1000 mL 5% Dextrose/Lactated Ringer's Recalled by...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 500 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pfizer Inc.

Recalled Item: Sterile Water for Injection Recalled by Pfizer Inc. Due to Non-Sterility:...

The Issue: Non-Sterility: cracked or chipped glass at the neck of Sterile Water for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 500 mL Lactated Ringer's Injection USP in 500 mL...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund