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. 2,371 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,371 in last 12 months

Showing 2624126260 of 48,326 recalls

Medical DeviceJanuary 29, 2018· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...

The Issue: The device may process the same sample with two different sample IDs and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging...

The Issue: The application may underestimate the EROA (Effective Regurgitant Orifice...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: Ray Station 4.9 Ray Station 5 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software issue with Center Beam in Field functionality. Issue can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Stryker Communications

Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...

The Issue: The mounts on the monitor may have an insufficient (missing or incomplete) weld.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph Horizon - PET/CT Recalled by Siemens Medical Solutions USA, Inc....

The Issue: Error introduced into PET images acquired and reconstructed with VJ20A...

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

Class II — Potential Health HazardOngoing
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel250 (flavocoxid and citrated zinc bisglycinate) 250 mg/50 mg capsules...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel (flavocoxid 500 mg) capsules Recalled by Primus Pharmaceuticals,...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel (flavocoxid 250 mg) capsules Recalled by Primus Pharmaceuticals,...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel500 (flavocoxid and citrated zinc bisglycinate) 500 mg/50 mg capsules...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 26, 2018· bioMerieux, Inc.

Recalled Item: bioMerieux VITEK 2 Gram Positive Cefoxitin Screen Recalled by bioMerieux,...

The Issue: Customer reports indicated an increase in the rate of non-detected MRSA in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 25, 2018· GE Healthcare

Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity...

The Issue: Potential that one or more image series may be missing from an exam without...

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

Class II — Potential Health HazardOngoing
DrugJanuary 25, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets...

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 25, 2018· Coblentz Distributing Inc dba Walnut Creek Foods

Recalled Item: WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Recalled by Coblentz...

The Issue: The firm was notified by the Ohio Dept. of Agriculture that they failed to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...

The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2018· GE Healthcare

Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...

The Issue: Potential that one or more image series may be missing from an exam without...

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

Class II — Potential Health HazardOngoing