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 4538145400 of 48,326 recalls

DrugMarch 7, 2013· Novartis Consumer Health

Recalled Item: 4 way Saline Moisturizing Mist with Eucalyptol & Menthol Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2013· Novartis Consumer Health

Recalled Item: Nupercainal Recalled by Novartis Consumer Health Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2013· Novartis Consumer Health

Recalled Item: 4 way Nasal Decongestant Menthol Nasal Spray Recalled by Novartis Consumer...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2013· Novartis Consumer Health

Recalled Item: 4 way Nasal Decongestant Fast Acting Nasal Spray Recalled by Novartis...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2013· Novartis Consumer Health

Recalled Item: Myoflex (trolamine salicylate) 10% Recalled by Novartis Consumer Health Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 7, 2013· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet Getinge Group battery modules for use with Maquet SERVO-i Recalled by...

The Issue: When using the SERVO-i on battery power, in a very small number of cases,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 7, 2013· Maquet Cardiovascular, LLC

Recalled Item: MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version...

The Issue: It has come to the attention of MAQUET that there have been episodes of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2013· US Endoscopy Group Inc

Recalled Item: Torrent" irrigation tubing. Product Usage: The Torrent irrigation system...

The Issue: The firm was notified by their customers that there was a water leakage from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Advanced Orthogonal Equipment, Incorporated

Recalled Item: Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a...

The Issue: Unapproved medical device

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1...

The Issue: Customer complaint investigation confirmed the issue of false skipped wells...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Alere San Diego, Inc.

Recalled Item: The Alere Cholestech LDX¿ high sensitivity C-Reactive Protein (hsCRP) Test...

The Issue: The Alere Cholestech LDX¿ hsCRP cassette (PN 12-807) may have increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Smith & Nephew Inc

Recalled Item: TRIGEN (TM) L-P SCREW Recalled by Smith & Nephew Inc Due to One batch of 4.5...

The Issue: One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner. Used...

The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner....

The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....

The Issue: The recall was initiated because Alere San Diego has an update for the Alere...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Carefusion Corporation

Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...

The Issue: The recall was initiated because Carefusion has received reports of a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 6, 2013· Carefusion Corporation

Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...

The Issue: The recall was initiated because Carefusion has identified potential risk...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2013· Zydus Pharmaceuticals USA Inc

Recalled Item: Venlafaxine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...

The Issue: Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2013· Stryker Endoscopy

Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...

The Issue: In certain operating room environments, a colored screen image occurs with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2013· Stryker Endoscopy

Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...

The Issue: In certain operating room environments, a colored screen image occurs with...

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

Class II — Potential Health HazardOngoing