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. 2,522 recalls have been distributed to Kansas in the last 12 months.
Showing 17561–17580 of 50,117 recalls
Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...
The Issue: The firm registered the product as a Class I device, but has since been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...
The Issue: Connector between support surface and pump may be out of tolerance resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...
The Issue: An update to the carryover avoidance technical bulletin to introduce...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Dehydrogenase L-P Recalled by Randox Laboratories Ltd. Due to An...
The Issue: An update to the carryover avoidance technical bulletin to introduce...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Aurobindo Pharma USA...
The Issue: Presence of Foreign Substance: product complaints were received by the firm...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elitek (rasburicase) for injection Recalled by Sanofi-Aventis U.S. LLC Due...
The Issue: Failed Stability Specifications: Out of Specification result for enzyme...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisone Tablets Recalled by Lannett Company, Inc. Due to Labeling: Label...
The Issue: Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Whole Foods Market Mitica La Dama Sagrada Raw Milk - Recalled by Whole Foods...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market Chimay Biere PLU 29351700000 Individual sliced cheese...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market Chimay Grand Cru PLU 29388800000 and Whole Recalled by...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market Artequeso Manchego 6 month aged raw Raw Recalled by Whole...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.