Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,558 recalls have been distributed to Arkansas in the last 12 months.
Showing 14841–14860 of 28,355 recalls
Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Smooth Recalled by...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Pressure Sentinel¿ Intramedullary Reaming System Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Humeral Guide Wire - Ball Tip Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Pressure Sentinel¿ Intramedullary Reaming System Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire - Bullet Tip Recalled...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System -PS Open Box Femoral Left Recalled by Zimmer Biomet,...
The Issue: Label on the outer carton or the patient labels does not match label on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System -PS Open Box Femoral Right Recalled by Zimmer Biomet,...
The Issue: Label on the outer carton or the patient labels does not match label on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...
The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q.zen biplane with Material 10848355 - a Angiographic x-ray Recalled...
The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q biplane with Material 10848282- - a Angiographic x-ray Recalled by...
The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS zee biplane systems with Material 10094141- a Angiographic x-ray...
The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...
The Issue: Falsely elevated (false positive) urobilinogen patient results due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 6 Slice (Air) Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 40 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Slice (Power) Recalled by Philips Medical Systems (Cleveland)...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.