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. 2,509 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,509 in last 12 months

Showing 1802118040 of 50,117 recalls

Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· TELEFLEX MEDICAL INC

Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...

The Issue: Potential for sterile packaging to be compromised¿

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· Hill-Rom, Inc.

Recalled Item: Progressa Bed Recalled by Hill-Rom, Inc. Due to Affected beds may have...

The Issue: Affected beds may have screws installed that do not meet material tensile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· Medline Industries Inc

Recalled Item: ClearPro Trach T-Piece Closed Suction Catheter Recalled by Medline...

The Issue: There are reports of the suction catheter coming apart from the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· Hill-Rom, Inc.

Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to Affected beds may...

The Issue: Affected beds may have screws installed that do not meet material tensile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· Medline Industries Inc

Recalled Item: ClearPro T-Piece Closed Suction Catheter Recalled by Medline Industries Inc...

The Issue: There are reports of the suction catheter coming apart from the device...

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

Class II — Potential Health HazardOngoing
DrugJune 29, 2020· Transliquid Technologies, LLC

Recalled Item: Mystic Shield PROTECTION Recalled by Transliquid Technologies, LLC Due to...

The Issue: Chemical Contamination: Presence of Undeclared Methanol

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 29, 2020· EMD Serono, Inc.

Recalled Item: Cetrotide (cetrorelix acetate for Injection) 0.25 mg Recalled by EMD Serono,...

The Issue: Defective Container: Market complaints of missing rubber stoppers from drug...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 29, 2020· Vitamin Shoppe

Recalled Item: The Vitamin Shoppe Calcium Citrate Plus Magnesium & Vitamin D. Recalled by...

The Issue: Sample analysis revealed product is sub-potent for Vitamin D

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 29, 2020· Garland Ventures, LTD DBA Bally Plus

Recalled Item: Freshness Guaranteed Five Cheese Stuffed Shells Traditional Italian Ricotta...

The Issue: Potential contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 29, 2020· Smith & Nephew, Inc.

Recalled Item: PERI-LOC TARGETER 4.5MM DISTAL FEMUR Recalled by Smith & Nephew, Inc. Due to...

The Issue: The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· Precision Valve & Automation,Inc

Recalled Item: PVA Recalled by Precision Valve & Automation,Inc Due to While operating the...

The Issue: While operating the machine in "Run" mode an unexcepted event may occur...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· Boss Instruments, Ltd.

Recalled Item: BOSS DeBakey "Gator-Grip" Needle Holder 2 mm tip Recalled by Boss...

The Issue: The tungsten carbide plate, which is intended to hold the sewing needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· RANDOX LABORATORIES, LTD.

Recalled Item: Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage:...

The Issue: Randox have confirmed imprecision of quality control and patient samples...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· RANDOX LABORATORIES, LTD.

Recalled Item: Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: Recalled...

The Issue: Randox have confirmed imprecision of quality control and patient samples...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· RANDOX LABORATORIES, LTD.

Recalled Item: Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Recalled...

The Issue: Randox have confirmed imprecision of quality control and patient samples...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· Steris Corporation

Recalled Item: InnoWave Sonic Irrigator Recalled by Steris Corporation Due to A recent FDA...

The Issue: A recent FDA inspection at the firm identified that the foil test performed...

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

Class II — Potential Health HazardOngoing
DrugJune 25, 2020· POLARIZED LLC

Recalled Item: Saniderm ADVANCED HAND SANITIZER Recalled by POLARIZED LLC Due to Undeclared...

The Issue: CGMP Deviations: Product was found to be below the label claim for ethanol...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 25, 2020· Philips North America, LLC

Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America, LLC...

The Issue: The device may experience an interruption of gas measurement due to a...

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

Class II — Potential Health HazardOngoing
DrugJune 24, 2020· Medichem S.A.

Recalled Item: Chlorhexidine Gluconate 0012 For Manufacturing Recalled by Medichem S.A. Due...

The Issue: Microbial contamination of Non-Sterile Product; detection of the...

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

Class I — Serious Health HazardOngoing
Refund