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. 2,440 recalls have been distributed to Kansas in the last 12 months.
Showing 23361–23380 of 50,117 recalls
Recalled Item: Wire Guide Recalled by Cook Inc. Due to The wire guide may be incorrectly...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide Recalled by...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bentson PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kwart Retro-Inject Ureteral Stent Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sof-Flex Multi-Lenqth Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heavy Duty PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to...
The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 10 mg* Recalled by Sun Pharmaceutical...
The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials Recalled...
The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: CGMP Deviations: Product complaints received indicating reconstituted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...
The Issue: Lack of Assurance of Sterility: Confirmed customer complaints for leaks on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: CGMP Deviations: Product complaints received indicating reconstituted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.