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. 2,476 recalls have been distributed to Kansas in the last 12 months.
Showing 18961–18980 of 50,117 recalls
Recalled Item: The CF-70 instrument (product code: LXG Recalled by Sysmex America, Inc. Due...
The Issue: Software mismatch-When the software versions between the SP-50 and CF-70 are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC...
The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...
The Issue: Undeclared yellow # 5 and blue # 1
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AVE 2 Birthing Bed - Product Usage: is designated to Recalled by Linet...
The Issue: The UDI on the device label indicates incorrect manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemLung Kit - DL31 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A17 Recalled...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart Pump Kit Recalled by Cardiac Assist, Inc Due to Failure to prime...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL3 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemLife Kit Product: 5740-0000...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL31 RD Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15 Recalled...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRx4841A 1.4 GHz IntelliVue Tele TRX Recalled by Philips North America, LLC...
The Issue: The ECG signal from patients being monitored using a Philips TRx4841A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRx4851A 2.4 GHz IntelliVue Tele TRX Recalled by Philips North America, LLC...
The Issue: The ECG signal from patients being monitored using a Philips TRx4841A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phillips Azurion 7 M20 Recalled by Philips North America, LLC Due to No...
The Issue: No torque was specified for the four screws that connect the gearbox and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices s intended to be used Recalled...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips V60 Ventilators with Power Management PCBA part number 1055906...
The Issue: Solder connection failure on Power Management printed circuit board assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: natus newborn care Olympic Brainz Monitor Recalled by Natus Neurology DBA...
The Issue: The OBM system functional test (impedance and noise) was not carried out on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.