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. 2,278 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,278 in last 12 months

Showing 4610146120 of 48,219 recalls

DrugOctober 22, 2012· Zi Xiu Tang Success, LLC

Recalled Item: Ultimate Formula Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 22, 2012· Zi Xiu Tang Success, LLC

Recalled Item: Classic Zi Xiu Tang Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Zenchent (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Necon 10/11 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Necon 1/35-28 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Lutera (levonorgestrel and ethinyl estradiol) Tablets USP Recalled by Watson...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 19, 2012· American Medical Systems, Inc.

Recalled Item: AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling Recalled by...

The Issue: American Medical Systems¿ (AMS) is issuing a voluntary recall on a number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Trivascular, Inc

Recalled Item: TriVascular brand Fill Polymer Kit Recalled by Trivascular, Inc Due to...

The Issue: Selected lots of the Fill Polymer Kit (European Model Number: TVFP14- B) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Innovative Magnetic Resonance Imaging Systems Inc.

Recalled Item: IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00)...

The Issue: IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· TITAN SPINE, LLC

Recalled Item: Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard...

The Issue: Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2012· OrthoPediatrics Corp

Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...

The Issue: Complaint received from sales representative that the drill guide tubes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2012· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Sliced CT Scanner System Recalled by Philips And Neusoft...

The Issue: The four screws that secure the patient table top to the carrier pulled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2012· Biomerieux Inc

Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...

The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...

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

Class II — Potential Health HazardOngoing
FoodOctober 17, 2012· Energy Club Inc

Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...

The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 17, 2012· Energy Club Inc

Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...

The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 16, 2012· PureFit Inc

Recalled Item: PureFit Peanut Butter Bars Recalled by PureFit Inc Due to Potential...

The Issue: PureFit is recalling PureFit Peanut Butter Crunch Bars because of possible...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 16, 2012· Mondelez Global Llc

Recalled Item: Green & Black's Organic Peanut & Sea Salt Milk Chocolate Recalled by...

The Issue: Mondelez Global LLC (Mondelez Global) is voluntarily recalling the U.S....

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...

The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...

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

Class II — Potential Health HazardOngoing