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 4558145600 of 48,326 recalls

Medical DeviceFebruary 11, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....

The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2013· Watson Laboratories Inc

Recalled Item: Meprobamate Recalled by Watson Laboratories Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 8, 2013· Watson Laboratories Inc

Recalled Item: Meprobamate Recalled by Watson Laboratories Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 8, 2013· Qtrade Teas And Herb

Recalled Item: Organic Lemon Grass Tea Bag Cut (TBC) Recalled by Qtrade Teas And Herb Due...

The Issue: QTrade Teas & Herbs is recalling Organic Lemon Grass Tea Bag Cut (TBC)...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...

The Issue: There is a potential for lead damage due to the use of the lead cap provided...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 8, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...

The Issue: There is a potential for lead damage due to the use of the lead cap provided...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 8, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare LOGIQ S8 (with software revisions R1.1.1 and R1.5.1) Recalled...

The Issue: GE Healthcare has become aware of a potential safety issue due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2013· Zimmer, Inc.

Recalled Item: Zimmer NexPosure Recalled by Zimmer, Inc. Due to Possibility that the inner...

The Issue: Possibility that the inner pouch may be compromised. The product is packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2013· Ultradent Products, Inc.

Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...

The Issue: Orthodontic brackets distributed was incorrectly labeled.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 7, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Ortho-Clinical...

The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2013· AGFA Corp.

Recalled Item: CR MD1.0 General Set Recalled by AGFA Corp. Due to The cassettes were...

The Issue: The cassettes were shipped with the wrong IP (image plate) size bar code.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2013· Ebi, Llc

Recalled Item: Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number Recalled...

The Issue: Increased risk of failure at the driver tip during screw insertion or removal.

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

Class II — Potential Health HazardOngoing
FoodFebruary 6, 2013· Pan -O- Gold Baking Co

Recalled Item: Rye bread with the following brands: Village Hearth Recalled by Pan -O- Gold...

The Issue: A recall has been initiated by Pan-O-Gold Baking Co. after they were...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Recalled by Hospira...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump. List Number 11971. The Plum A+ Recalled by Hospira...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump with Hospira MedNet Software. List Number Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing