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. 2,053 recalls have been distributed to Kansas in the last 12 months.
Showing 4681–4700 of 50,117 recalls
Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Pump Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump 371 14F LT CMR Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 Set AU Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Reser's Fine Foods, Inc. Due to Foreign Object Contamination
The Issue: Foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Recalled by Reser's Fine Foods, Inc. Due to Foreign Object Contamination
The Issue: Foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Recalled by Reser's Fine Foods, Inc. Due to Foreign Object Contamination
The Issue: Foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Recalled by Reser's Fine Foods, Inc. Due to Foreign Object Contamination
The Issue: Foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Recalled by Reser's Fine Foods, Inc. Due to Foreign Object Contamination
The Issue: Foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Recalled by Reser's Fine Foods, Inc. Due to Foreign Object Contamination
The Issue: Foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Empower Pharmacy Recalled by EMPOWER CLINIC SERVICES LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monarch Platform (Endoscopy) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform (Urology) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAGNUM Disposable Core Tissue Biopsy Needle MN Recalled by Bard...
The Issue: Due to possible packaging damage (indentations/cuts) cause by manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.