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. 2,465 recalls have been distributed to Kansas in the last 12 months.
Showing 19841–19860 of 50,117 recalls
Recalled Item: Reinforced Introducer Sets Maquet 7.5 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by AuroMedics Pharma LLC Due to Presence of...
The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...
The Issue: Lack of Assurance of Sterility: Product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP)...
The Issue: Atellica and ADVIA hsCRP calibrator accuracy has drifted away from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH High Sensitivity C-Reactive Protein (HsCRP) Calibrator - Product...
The Issue: Atellica CH: The Atellica¿ CH High Sensitivity CReactive Protein Calibrator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...
The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT Recalled by...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD HDR Recalled by Angiodynamics, Inc. Due to May result in readings...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD Electron Recalled by Angiodynamics, Inc. Due to May result in...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD EXTERNAL BEAM PHOTON Recalled by Angiodynamics, Inc. Due to May...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system Recalled by...
The Issue: Editing a static arc beam may unexpectedly set the MU of the beam to its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA SYSTEM CONROL N + P (ref. 00678) Recalled by Diagnostica Stago, Inc. Due...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA UNICALIBRATOR (ref. 00675) Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elasto-Gel Absorbent Wound Dressing Recalled by Southwest Technologies Inc...
The Issue: Elasto-Gel Wound Dressing may be contaminated with mold.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Polymer Detection Kit Recalled by Leica Microsystems, Inc. Due to BOND...
The Issue: BOND Polymer Detection kits (DS9800) were held out of storage longer than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.