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. 2,334 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,334 in last 12 months

Showing 3750137520 of 48,326 recalls

Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Delivery/C-Section Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Hysto Pack Recalled by Covidien LLC Due to Devon Light Gloves contain splits...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Surgical Set Up kit Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· BioHorizons Implant Systems Inc

Recalled Item: Tapered HD Upgrade Set Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: BioHorizons Tapered HD Upgrade set was packaged with an incorrect drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Major Kit Recalled by Covidien LLC Due to Devon Light Gloves contain splits...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Augmentation Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Non Sterile Subassembly: Catalog Number/Description: SA1008 NONSTERILE...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Mallory/Head Primary Hip System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Double Basin Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Minor Surgical Kits Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Biomet Cobalt-Chrome Femoral Components Recalled by Biomet, Inc. Due to...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: NS-3600-B LITE GLOVE 1000/CASE -Bulk Recalled by Covidien LLC Due to Devon...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
DrugApril 16, 2015· Tarmac Products, Inc.

Recalled Item: Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle...

The Issue: Products failed the Antimicrobial Effectiveness Test

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 16, 2015· Tarmac Products, Inc.

Recalled Item: Well at Walgreens Regular Strength Comfort Gel Cherry Flavor Recalled by...

The Issue: Products failed the Antimicrobial Effectiveness Test

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 16, 2015· Tarmac Products, Inc.

Recalled Item: Well at Walgreens Regular Strength Antacid Liquid Recalled by Tarmac...

The Issue: Products failed the Antimicrobial Effectiveness Test.

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

Class II — Potential Health HazardOngoing
Refund