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 2698127000 of 48,326 recalls

FoodOctober 6, 2017· Bel Brands USA

Recalled Item: Merkts Port Wine Cheese Spread Recalled by Bel Brands USA Due to Bel Brands...

The Issue: Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2017· CooperSurgical, Inc.

Recalled Item: Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical...

The Issue: The 2MHZ prove was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2017· Purdue Pharma, LP

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...

The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2017· Monteris Medical Corp

Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...

The Issue: The firm received complaints that involved an unanticipated interaction...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...

The Issue: Firewall installed with Philips IntelliVue Information Center iX or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...

The Issue: While reviewing documentation for the next software release of the 2008T, an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Teleflex Medical

Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...

The Issue: The product has a non-conformity that may cause clips to mislead, jam or...

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

Class II — Potential Health HazardOngoing
DrugOctober 3, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Famotodine has an out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 3, 2017· Becton Dickinson & Co.

Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling

The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.

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

Class II — Potential Health HazardOngoing
DrugOctober 2, 2017· Unichem Pharmaceuticals Usa Inc

Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...

The Issue: The table may become unstable if the nuts on the bolts were not adequately...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...

The Issue: The table may become unstable if the nuts on the bolts were not adequately...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2017· Edwards Lifesciences, LLC

Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...

The Issue: Pre-procedural issues related to software defects

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2017· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...

The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...

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

Class II — Potential Health HazardOngoing
FoodSeptember 29, 2017· Pinnacle Food Group, Llc

Recalled Item: Birds Eye Baby Sweet Peas Recalled by Pinnacle Food Group, Llc Due to...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 29, 2017· Tai Foong USA Inc

Recalled Item: Costco item # 1052939 Recalled by Tai Foong USA Inc Due to Undeclared Egg

The Issue: Royal Asia brand Shrimp Wonton Noodle Soup is recalled due to undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...

The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...

The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.

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

Class II — Potential Health HazardOngoing