Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,277 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,277 in last 12 months

Showing 4562145640 of 48,326 recalls

Medical DeviceFebruary 4, 2013· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...

The Issue: Incorrect packaging of regular set and fast set cartridges.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 4, 2013· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...

The Issue: Incorrect packaging of regular set and fast set cartridges.

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

Class III — Low RiskOngoing
DrugFebruary 1, 2013· Ferring Pharmaceuticals Inc

Recalled Item: TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Recalled...

The Issue: Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 1, 2013· Fresenius Kabi USA LLC (FK USA)

Recalled Item: CALCIUM GLUCONATE INJECTION Recalled by Fresenius Kabi USA LLC (FK USA) Due...

The Issue: Labeling: Missing label

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Hyperbaric Infusion System is a cassette based Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing