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. 2,610 recalls have been distributed to Kansas in the last 12 months.
Showing 5721–5740 of 28,538 recalls
Recalled Item: ADVIA Chemistry Iron_2 (IRON_2) Reagents Recalled by Siemens Healthcare...
The Issue: There is a potential for a positive bias on Quality Control (QC) and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartmate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to Inability to...
The Issue: Inability to start and/or complete the coring procedure due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B.Braun NORM-JECT Luer Lock Solo Recalled by B. Braun Medical, Inc. Due to...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B. Braun NORM-JECT Luer Solo Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing): 180-Gram Cement Cartridge with...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT Chemistry Products ALKP Slides Recalled by Ortho-Clinical...
The Issue: Samples containing high levels of ALKP (or an interfering substance) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides Recalled by Ortho-Clinical...
The Issue: Samples containing high levels of ALKP (or an interfering substance) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: Empowr Knee Recalled by Encore Medical, LP Due to Orthopedic...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: Delta Ceramic Femoral Head Recalled by Encore Medical, LP Due...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: CLP Hip Recalled by Encore Medical, LP Due to Orthopedic...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: Reverse Shoulder System (RSP) Semi Humeral Socket Insert...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.