Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,447 recalls have been distributed to Iowa in the last 12 months.
Showing 26321–26340 of 49,990 recalls
Recalled Item: Whole Wheat Chocolate Animal Cookies Recalled by NatureBox, Inc. Due to...
The Issue: While packing from a bulk bin of whole wheat chocolate animal cookies, 2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mitragyna Speciosa Leaf Powder-GREEN Horn Recalled by Viable Solutions, LLC...
The Issue: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mitragyna Speciosa Leaf Powder-Thai Maeng Da Recalled by Viable Solutions,...
The Issue: Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...
The Issue: There is a potential for the cord to spark and cause a fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only...
The Issue: Failed Dissolution Specification: Low dissolution outside of specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...
The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Peaceful Mountain Recalled by Grato Holdings, Inc. Due to Multiple products...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southwestern Gourmet Butter Popcorn Grand Canyon Foods Recalled by Grand...
The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southwestern Gourmet Prickly Pear Popcorn Grand Canyon Foods Recalled by...
The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peaceful Mountain -Stomach Rescue - Dietary supplement - Elemental silver...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Quadra Assura MP Recalled by St Jude Medical Inc. Due to The firm is...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Current Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.