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. 2,428 recalls have been distributed to Iowa in the last 12 months.
Showing 33621–33640 of 49,990 recalls
Recalled Item: Product is packaged into a plastic bag and placed into Recalled by Woodland...
The Issue: Sunflower seeds purchased from SunOpta that are potentially contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product is packed in a corrugated box with poly line Recalled by Tarrier...
The Issue: The firm was notified by their supplier that the products may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical portio adapter (acorn) small & large are used for Recalled by...
The Issue: The distal end of the Conical portio adapter (acorn) is composed of a small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...
The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Delayed-release Tablets USP Recalled by Teva North America...
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...
The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.