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. 2,285 recalls have been distributed to Wyoming in the last 12 months.
Showing 43141–43160 of 48,219 recalls
Recalled Item: Olde Cape Cod Chipotle Ranch dressing Recalled by Cains Foods L.P. Due to...
The Issue: Product may be labeled with an incorrect back panel label that does not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product Name: AVEA¿ Ventilator. All Models. The affected devices are...
The Issue: CareFusion has identified a potential risk associated with AVEA¿ ventilators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spironolactone tablets Recalled by Greenstone Llc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aldactone (spironolactone) tablets Recalled by Pfizer Us Pharmaceutical...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spironolactone tablets Recalled by Greenstone Llc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cranial Access (CRAK) Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra is recalling certain lots of Cranial Access Kit due to a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loratadine Recalled by Novartis Consumer Health Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: The products are being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: (Siemens Rad Fluoro Uro Systems) Ysio Recalled by Siemens Medical Solutions...
The Issue: A potential malfunction and hazard to patients exists when using the Ysio,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro system (Luminos dRF and Uroskop Omnia Recalled by...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1650 System Software: 1) V4.01 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1200 System Software: 1) V2.00 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1800 System Software V2.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2400 System Software V4.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creafuse Grape Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Creafuse Fruit Punch Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aminosyn II Recalled by Hospira Inc. Due to Presence of Particulate Matter:...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg...
The Issue: Presence of Foreign Substance: This recall is being conducted due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Watson...
The Issue: Defective Container: Defective bottles may not have tamper evident seals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GoPicnic Black Bean Dip & Plantain Chips Recalled by GoPicnic, Inc. Due to...
The Issue: The chocolates included in the meal kits may contain undeclared milk allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gopicnic Recalled by GoPicnic, Inc. Due to Undeclared Milk
The Issue: The chocolates included in the meal kits may contain undeclared milk allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.