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. 2,348 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,348 in last 12 months

Showing 3388133900 of 48,219 recalls

DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Ultimate Formula Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SLIM TRIM U Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: La' Trim Plus Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Infinity Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Jenesis Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Prime Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: XCEL ADVANCED Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: EVOLVE BEE POLLEN Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: XCEL Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared Fluoxetine

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Asset extreme+PLUS Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: ZI XIU TANG BEAUTY FACE & FIGURE Capsules Recalled by Bee Extremely Amazed...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Confirmed customer compliants of finding an...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Baxter Healthcare Corp.

Recalled Item: Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer compliants of finding an...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Lindane Lotion Recalled by Morton Grove Pharmaceuticals, Inc. Due to...

The Issue: Super-Potent Drug: Out of Specification Assay test results were reported for...

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

Class III — Low RiskOngoing
Refund
FoodDecember 15, 2015· Trader Joes Company

Recalled Item: Triple Ginger Brew Recalled by Trader Joes Company Due to Trader Joes...

The Issue: Trader Joes recalling Triple Ginger Brew due to reports of unopened bottles...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 15, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...

The Issue: An issue with the Panorama Central Station may cause the system to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...

The Issue: The door latch may not fully close and the door may open unexpectedly. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...

The Issue: On a rare occasion, there is a potential to assign a patient result to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing