Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,334 recalls have been distributed to Kansas in the last 12 months.
Showing 46741–46760 of 50,117 recalls
Recalled Item: Lloyd Thyro-Tab 0.125 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lloyd Thyro-Tab 0.100 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lloyd Thyro-Tab 0.137 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lloyd Thyro-Tab 0.175 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lloyd Thyro-Tab 0.200 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROCK-IT MAN capsules Recalled by Consumer Concepts, Inc. Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...
The Issue: Product is being recalled because the combination of the current 50 mg vial,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14219-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...
The Issue: The firm is recalling the specific lot due to lower than expected results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...
The Issue: In rare instances, channel shifted results have been generated with cobas¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.