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. 903 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
903 in last 12 months

Showing 46341–46360 of 48,219 recalls

FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Endurance Pre Race Pina Colada Recalled by Maine Natural Health, Inc. Due to...

The Issue: Protein supplement fails to declare allergens: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Endurance Daily Chocolate Dietary Supplement Packaged under the label:...

The Issue: Protein supplement fails to declare allergens milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Recovery Vanilla (also labeled Post Workout) Recalled by Maine Natural...

The Issue: Protein supplement fails to declare allergens: milk, shellfish

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Pure Whey Vanilla Recalled by Maine Natural Health, Inc. Due to Protein...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Daily Balance Chocolate Dietary Supplement Packaged under the labels...

The Issue: Protein supplement fails to declare allergen milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Hunger and Weight Chocolate Dietary Supplement Packaged under the labels...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Recovery Chocolate (also labeled Post Workout) Recalled by Maine Natural...

The Issue: Protein supplement fails to declare allergens: milk, shellfish

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Endurance In Race Coconut Dietary Supplement Packaged under the label...

The Issue: Protein supplement fails to declare allergens: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Fortified Chocolate Dietary Supplement Packaged under the labels Stronger...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 20, 2012· Globe All Wellness, LLC

Recalled Item: SLIM XTREME Herbal Slimming Capsule Recalled by Globe All Wellness, LLC Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL...

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL...

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2012· Sandoz Incorporated

Recalled Item: Children's Cetirizine HCl Chewable Tablets 5 mg Recalled by Sandoz...

The Issue: Impurity/Degradation; exceeded impurity specification at the 8 and 15 month...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 20, 2012· Captiva Spine, Inc

Recalled Item: CapLOX II Final Torque Driver Recalled by Captiva Spine, Inc Due to Captiva...

The Issue: Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Zimmer, Inc.

Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...

The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 200amx with digital upgrade Mobile general Recalled...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Medline Industries Inc

Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...

The Issue: The Back Table Cover component in the custom pack was placed in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Advanced Sterilization Products

Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...

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

Class II — Potential Health HazardOngoing