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 4534145360 of 48,326 recalls

FoodMarch 13, 2013· Daesang America Inc

Recalled Item: Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g Recalled by...

The Issue: Sesame and Garlic Flavored Mixed Soy Bean Paste contains peanut powder which...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 13, 2013· Epocal

Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...

The Issue: This recall is being initiated because the affected lots of this product may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Separation Technology, Inc.

Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...

The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Masimo Corporation

Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...

The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 2-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 6-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire Recalled by...

The Issue: Medtronic has identified an issue involving specific lot numbers of the...

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

Class II — Potential Health HazardOngoing
DrugMarch 12, 2013· L. Perrigo Co.

Recalled Item: Liothyronine Sodium Tablets Recalled by L. Perrigo Co. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: 3 month stability testing.

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

Class III — Low RiskOngoing
Refund
DrugMarch 12, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa (levonorgestrel/ethinyl estradiol) Tablets Recalled by Teva...

The Issue: Failed Tablet/Capsule Specifications: This recall is being carried out due...

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

Class III — Low RiskOngoing
Refund
DrugMarch 12, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Portia (levonorgestrel and ethinyl estradiol) Tablets Recalled by Teva...

The Issue: Failed Tablet/Capsule Specifications: This recall is being carried out due...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 12, 2013· Custom Ultrasonics, Inc.

Recalled Item: Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector....

The Issue: Certain System 83 Plus 2 and System 83 Plus 9 units running the Windows 7...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare has become aware of a potential safety issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Berchtold Corp.

Recalled Item: Hand Controls for Operon D750 Recalled by Berchtold Corp. Due to The firm...

The Issue: The firm received complaints for unintended movements.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16-Slice Water Recalled by Philips Medical Systems (Cleveland)...

The Issue: Philips Healthcare received a report from the field stating when they viewed...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2013· Green Planet Inc

Recalled Item: Night Bullet Capsules Recalled by Green Planet Inc Due to Marketed Without...

The Issue: Marketed Without an Approved NDA/ANDA; product contains analogues of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 11, 2013· Hi-Tech Pharmacal Co., Inc.

Recalled Item: Acetic Acid Otic Solution Recalled by Hi-Tech Pharmacal Co., Inc. Due to...

The Issue: Subpotent Drug: The product/lot is out-of-specification (OOS) for the assay...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2013· Gsms

Recalled Item: LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETS Recalled by Gsms Due to Presence...

The Issue: Presence of Foreign Substance: Reports of gray smudges identified as minute...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 11, 2013· Nashua Nutrition

Recalled Item: Proti Diet High Protein Chocolate Dream Bar Recalled by Nashua Nutrition Due...

The Issue: Product may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund