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. 1,854 recalls have been distributed to Kansas in the last 12 months.
Showing 25441–25460 of 28,538 recalls
Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR (various sizes) Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar liners and Multipolar cups with the following dimensions in MM (38...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude...
The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magna-Fx Cannulated Screw Fixation System 7.0 mm. Item codes starting...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX KEYLESS 90D X 8 and X 11 Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECON SCREW LG 5.5MM DIA and M/DN FEM IM NAIL Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...
The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 COMP PLT Recalled by Zimmer, Inc. Due to Zimmer recently conducted a...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISTAL MEDIAL FEMORAL CON Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZIMTRON 6 DEG 22 HEADS Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASIA ONE-PIECE LAG SCREW Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBERT BONE SCREW Recalled by Zimmer, Inc. Due to Zimmer recently conducted...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM HD ION (various sizes) Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN R-F IM NAIL 9MM DIA Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS HERITAGE FEM STEM Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II KEYLESS TUBE Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.