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. 1,019 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,019 in last 12 months

Showing 18281–18300 of 50,117 recalls

DrugJune 5, 2020· Marksans Pharma Limited

Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2020· Akorn, Inc.

Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...

The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 5, 2020· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 7mm implant component...

The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Verathon, Inc.

Recalled Item: GlideScope Core OneTouch Smart Cable Recalled by Verathon, Inc. Due to When...

The Issue: When video laryngoscopy system users apply, twisting motions while...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2020· HF Acquisition Co. LLC

Recalled Item: STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: Recalled...

The Issue: A missing component (hand suction pump) in the emergency medical kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics,...

The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Medtronic Navigation, Inc.

Recalled Item: StealthStation" S7 System with Polaris Spectra Camera part number PSU...

The Issue: There is a potential for specific camera units to be affected by a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 6mm implant component...

The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing Recalled...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: STAT KIT Recalled by HF Acquisition Co., LLC Due to Instead of 2 doses,...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Cardinal Health 200, LLC

Recalled Item: Cardinal Health NPWT Canister with Gel 300cc Recalled by Cardinal Health...

The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing