Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,342 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,342 in last 12 months

Showing 3524135260 of 48,219 recalls

DrugAugust 6, 2015· 3M Company - Health Care Business

Recalled Item: DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and...

The Issue: Chemical contamination: Product may be contaminated with a toxic compound.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2015· Caribou Coffee Company Inc.

Recalled Item: Caribou Chocolate Chip Toffee Pecan Biscotti Recalled by Caribou Coffee...

The Issue: Biscotti Almond and Biscotti Chocolate Chip Toffee Pecan are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2015· Caribou Coffee Company Inc.

Recalled Item: Caribou Almond Biscotti Recalled by Caribou Coffee Company Inc. Due to...

The Issue: Biscotti Almond and Biscotti Chocolate Chip Toffee Pecan are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2015· Biomet Microfixation, LLC

Recalled Item: Neuro Combo Set Case The cases hold surgical instrumentation in Recalled by...

The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Biomet Microfixation, LLC

Recalled Item: Thinflap System Case The cases hold surgical instrumentation in place...

The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· SynCardia Systems Inc.

Recalled Item: Temporary Total Artificial Heart (TAH-t) with Freedom Driver System by...

The Issue: SynCardia Systems, Inc. is recalling Freedom Drivers due to a specific...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: MAHURKAR"* 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2015· Taro Pharmaceuticals, Inc.

Recalled Item: Topicort (desoximetasone) Topical Spray Recalled by Taro Pharmaceuticals,...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund