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. 2,359 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,359 in last 12 months

Showing 3142131440 of 48,326 recalls

FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags Recalled by...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass .023" Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass RX Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Natus Medical Incorporated

Recalled Item: Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides...

The Issue: The firm sent the Technical Bulletin to consignees who received the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod Recalled by...

The Issue: RTI Surgical Inc. (RTI) is conducting a voluntary recall on two specific...

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

Class II — Potential Health HazardOngoing
DrugSeptember 16, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Marcaine 0.25% (bupivacaine HCl) injection Recalled by Hospira Inc., A...

The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Marcaine 0.5% (bupivacaine HCl) injection Recalled by Hospira Inc., A Pfizer...

The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2016· Pfizer Inc.

Recalled Item: PREMARIN (conjugated estrogen tablets Recalled by Pfizer Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 15, 2016· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...

The Issue: Image data for a patients image may not be correct

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...

The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Keystone Dental Inc

Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...

The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...

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

Class II — Potential Health HazardOngoing
FoodSeptember 15, 2016· Ferrara Candy Comp

Recalled Item: BRACH'S Chocolate Creations Recalled by Ferrara Candy Comp Due to Undeclared...

The Issue: Undeclared peanuts and wheat in product.

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

Class I — Serious Health HazardOngoing
Refund