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. 2,423 recalls have been distributed to Kansas in the last 12 months.
Showing 28521–28540 of 50,117 recalls
Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laceration Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomcat Instrument Recalled by Hologic, Inc Due to A Tomcat Instrument...
The Issue: A Tomcat Instrument software anomaly that causes the pipettor arm to make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Tiburon(R) Arthroscopy Drape Recalled by Cardinal Health 200,...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Under Buttocks Drape with Fluid Control Pouch II Recalled by...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Succinylcholine Chloride Injection (Preserved) 20 mg per mL Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.