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. 2,637 recalls have been distributed to Kansas in the last 12 months.
Showing 1261–1280 of 50,117 recalls
Recalled Item: ESPOCAN Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Set Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as Recalled by Pepsico...
The Issue: Undeclared sugar in finished product-primary package does not the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Azelaic Acid Gel Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP...
The Issue: CGMP Deviations: Market complaints received for gritty texture (grainy)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure Recalled...
The Issue: InSure ONE failed sensitivity testing when used with Test Card Lot T241102,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Software Builds 3.1.3 Recalled by ELEKTA...
The Issue: When appending a care plan that contains one or more wave medication orders,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent Recalled by Beckman...
The Issue: Beckman Coulter has identified that there is an increased probability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oral Probe (Product code 02893-000) Recalled by Baxter Healthcare...
The Issue: Affected oral/axillary probes were inadvertently programmed with the rectal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400...
The Issue: Instructions for use for a foot plating system is being updated to remove...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phasitron 5 Recalled by Percussionaire Corporation Due to IFU update;...
The Issue: IFU update; in-line valve, with pressure relief seal may leak when used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use...
The Issue: Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent: During long term stability testing of Levothyroxine Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Catalyft PL & PL40 Expandable Interbody System labeled as follows Recalled...
The Issue: Expandable interbody system cage may loose height or collapse (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.