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. 2,334 recalls have been distributed to Kansas in the last 12 months.
Showing 47541–47560 of 50,117 recalls
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT HBsAg Qualitative Assay Recalled by Abbott Laboratories, Inc Due...
The Issue: Abbott has identified that assay files for the ARCHITECT HBsAg Qualitative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For...
The Issue: The microelectrodes are not flush with the silastic substrate, may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE Diamond Pill Recalled by Performance Plus Marketing, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLUE Diamond PLATINUM Capsules Recalled by Performance Plus Marketing, Inc....
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mojo nights Capsules Recalled by Performance Plus Marketing, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CASANOVA Capsules Recalled by Performance Plus Marketing, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mojo nights SUPREME Capsules Recalled by Performance Plus Marketing, Inc....
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: libigrow capsules Recalled by Performance Plus Marketing, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: libigrow XXXTREME Capsules Recalled by Performance Plus Marketing, Inc. Due...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EXPAREL (bupivacaine liposome injectable suspension) Recalled by Pacira...
The Issue: Subpotent; bupivacaine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisone tablets Recalled by L. Perrigo Co. Due to Presence of Foreign...
The Issue: Presence of Foreign Substance(s); Perrigo has been notified of a recall by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.