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. 2,335 recalls have been distributed to Kansas in the last 12 months.
Showing 44461–44480 of 50,117 recalls
Recalled Item: enGen Track System with enGen Custom v3.2.2 (& below) Product The VITROS 5...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder...
The Issue: Complaints were received which described the SynFix LR implant holder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...
The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1) The HomeChoice automated peritoneal dialysis system. Dataplate located on...
The Issue: In systems with version 10.4 software Initial Drain logic, the device will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser Recalled by LAP...
The Issue: Potential for patient to be marked incorrectly. Customers currently using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: User Defined Method Flex Assignment/Siemens Dimension Vista 500 or Dimension...
The Issue: When utilizing the Routine Inventory screen to enter a User Defined Method...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Plus" 10mm x 12mm Webless implants Pioneer Surgical's C-Plus " Recalled by...
The Issue: As the result of a recent internal review of regulatory documents, we have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms)...
The Issue: Mindray has identified an issue with V Series Monitor where the V Dock power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....
The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm...
The Issue: A small number of units in lot number 0006573585 of the Resolute Integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....
The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digestive Health Recalled by Ultra Laboratories Due to Ultra Laboratories is...
The Issue: Ultra Laboratories is recalling Digestive Health because a raw material used...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VIT-RA-TOX Whole Beet Plant Juice Recalled by Vitalab Co Inc Due to Foreign...
The Issue: The firm reports a customer found a foreign object in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VITROS Chemistry Products COCM Reagent Recalled by Ortho-Clinical...
The Issue: Inaccurate quality control results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Market Pantry brand Animal Cookies Recalled by D. F. Stauffer Biscuit Co,...
The Issue: undeclared milk and egg in Market Pantry brand white fudge coated Animal Cookies
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: XYLANASE 150 Recalled by Specialty Enzymes & Biotechnologies Due to...
The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protease: APEX 10-7082 CENTURY 7-152 EB 2-14511 EB 5-16901 EB Recalled by...
The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...
Recommended Action: Do not consume. Return to store for a refund or discard.