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. 1,103 recalls have been distributed to Wyoming in the last 12 months.
Showing 861–880 of 48,219 recalls
Recalled Item: IntelliVue Patient Monitor MX550. Product Number: 866066. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phytonadione Injectable Emulsion Recalled by Cipla Limited Due to Failed...
The Issue: Failed Stability Specifications: Observed OOS results: eg results for colour...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus OER-Pro Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3% Polocaine DENTAL Recalled by Novocol Pharmaceutical of Canada, Inc. Due...
The Issue: Defective container: cracked/broken cartridges
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 2% Xylocaine DENTAL with Epinephrine 1:100 Recalled by Novocol...
The Issue: Defective container: cracked/broken cartridges
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus OER-Mini Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP20. Product Number: M8001A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP5. Product Number: M8105A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Premium Kratom Bali Gold powder is packaged in seal Recalled by...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Premium Kratom Red Bali powder is packaged in seal Recalled by Lotus...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Premium Kratom White Elephant powder is packaged in seal Recalled by...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Premium Kratom Green Maeng Da powder is packaged in Recalled by...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...
The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...
The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic Recalled by...
The Issue: Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Recommended Action: Do not consume. Return to store for a refund or discard.