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. 2,341 recalls have been distributed to Kansas in the last 12 months.
Showing 2081–2100 of 28,538 recalls
Recalled Item: Proxima Drape labeled as PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape. Recalled...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as FACE LIFT. Sterile surgical drape. Recalled by...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW Recalled by MEDLINE...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: PML Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zebra Thermal Barcode Printer GX430t Recalled by Remel, Inc Due to Power...
The Issue: Power supply unit for Zebra Printers used with the device can potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z1 Femoral Hip System Recalled by Zimmer, Inc. Due to There is a potential...
The Issue: There is a potential design issue with the Z1 Offset Stem Inserter leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: MTS Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: 1) MTS Recalled by MEDLINE INDUSTRIES, LP...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) AOP/BASIC EYE PACK-LF Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CV NEONATAL PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ACL ARTHROSCOPY PACK Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) BILLINGS CLINIC SC HEAD & NECK...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CSMC/ABDOMINAL HYST PACK-LF Recalled...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.