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. 1,090 recalls have been distributed to Kansas in the last 12 months.
Showing 8501–8520 of 28,538 recalls
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) JOBST Compri2 Recalled by BSN Medical Inc Due to Mislabeling
The Issue: The folding boxes within the shipping case are mislabeled. The shipping case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N Recalled by...
The Issue: Malfunction of the hand pendant controlling movement of the therapy couch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dispensing Pins for Air Inlet Filter Recalled by B. Braun Medical, Inc. Due...
The Issue: This lot may have an elevated risk of leakage from the Air-Inlet Filter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysiosystem with VC10 software version Recalled by Siemens Medical Solutions...
The Issue: Siemens Healthineers has identified a software error in previous software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V. For radiographic and fluoroscopic studies and intervention....
The Issue: The fluoroscopic dose rate might exceed the conforming value during biplane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STANDARD Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Recalled by SD...
The Issue: Illegal importation of COVID-19 AG Test kits into the U.S. The COVID-19 Ag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS Recalled by Remote Diagnostic Technologies Ltd. Due to...
The Issue: Distribution of Defibrillators that are not approved or cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated)...
The Issue: If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....
The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....
The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material #...
The Issue: Dimension Vista Magnesium Flex reagent cartridge lots exhibiting imprecision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler USA Recalled by Brasseler USA, Medical L.L.C. Due to One lot of...
The Issue: One lot of product was distributed in unsealed packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E25Bio COVID-19 Direct Antigen Rapid Test Recalled by E25Bio, Inc. Due to...
The Issue: The Test is not authorized, cleared, or approved by FDA for clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.