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 7761–7780 of 28,538 recalls
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4564 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6535 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Scope Introducer Catalog Number: 4650 Recalled by Hobbs Medical, Inc....
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 7202 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4814 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4720 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544)...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORCA FOAM STANDARD CUBE 10x10x10 mm Recalled by GELITA MEDICAL GMBH Due to...
The Issue: In routine bioburden testing, higher than acceptable levels of Endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone Recalled...
The Issue: An incorrect sizing label was applied to the carton packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute...
The Issue: (1)Software version 2.74 upgrade and (2)hardware related cause that affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco Medical Network Adapter Recalled by BARCO NV Due to installation issues
The Issue: installation issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diasol Acid Concentrate 100 Recalled by Diasol, Inc Due to Due to labeling...
The Issue: Due to labeling issue. The box label is different that the gallon label in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT STAT Troponin-I Reagent Kit Recalled by Abbott Laboratories Due to...
The Issue: One lot of reagent was manufactured with insufficient quantities of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.