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. 2,522 recalls have been distributed to Kansas in the last 12 months.
Showing 17541–17560 of 50,117 recalls
Recalled Item: Amiodarone Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Speed Stitch Needle Cassette Recalled by ArthroCare Corporation Due to Due...
The Issue: Due to a supplier error where a portion of the raw material was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: Chemical Contamination: FDA analysis found the product contains methanol,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: CGMP Deviations: All other lots are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump Recalled...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine HCl Injection Recalled by Hikma Pharmaceuticals USA Inc. Due...
The Issue: Sub-potent Drug: Out-of-Specification assay results found at 3 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NM/CT 850 Model Number: H3907AD Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Model # H3101RH Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Model # H3100AS Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM670 Pro Model # H3100XB Recalled by GE Healthcare, LLC Due to...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 CZT Model # H3906CW Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM 830 Model # H3910AC Recalled by GE Healthcare, LLC Due to Rotor bearing...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery 670 DR Model # H3100BT Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Recalled by GE Healthcare, LLC Due to Rotor bearing screws were...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...
The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...
The Issue: Masks processed at one site were not maintained at levels of condensation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...
The Issue: Due to non-surgical isolation gowns not meeting all performance test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.