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. 2,598 recalls have been distributed to Kansas in the last 12 months.
Showing 7441–7460 of 50,117 recalls
Recalled Item: Trospium Chloride Extended-Release Capsules Recalled by Padagis US LLC Due...
The Issue: Failed Tablets/Capsules specifications; missing/broken/extra tablets within...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...
The Issue: A software issue where "low" and "terminal" battery alerts did not display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Oasis Drain Single W / AC Recalled by Atrium Medical Corporation Due...
The Issue: A sterilization nonconformance prematurely aged the product by 48.3 days,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4...
The Issue: Under certain circumstances, information from HL7 messages received by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump...
The Issue: In affected products, the tubing outer diameter may vary in size or the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400 Recalled by Cardinal...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by The Harvard Drug...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol Recalled by Cardinal...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.