Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,263 recalls have been distributed to Rhode Island in the last 12 months.
Showing 45841–45860 of 47,970 recalls
Recalled Item: The Siemens Symbia T series is intended to aid in detecting Recalled by...
The Issue: There is a potential for the linear bearing car to fail allowing the ball...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Siemens Symbia S series is intended to aid in detecting Recalled by...
The Issue: There is a potential for the linear bearing car to fail allowing the ball...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem Recalled by Stryker...
The Issue: Stryker has received a report that single size 3.5 stem was packaged as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultimate Formula Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Classic Zi Xiu Tang Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEXTEND 6% Hetastarch in Lactated Electrolyte Injection Recalled by Hospira...
The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alere Cholestech LDX Calibration Verification Recalled by Alere San Diego,...
The Issue: Out of range (increased) HDL Cholesterol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Multianalyte Control Recalled by Alere San Diego, Inc....
The Issue: Out of range (increased) HDL Cholesterol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Taxo XV Factor Strips Recalled by Becton Dickinson & Co. Due to In...
The Issue: In vitro diagnostic test kit was not manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Necon 10/11 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lutera (levonorgestrel and ethinyl estradiol) Tablets USP Recalled by Watson...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Necon 1/35-28 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenchent (norethindrone and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard...
The Issue: Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00)...
The Issue: IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriVascular brand Fill Polymer Kit Recalled by Trivascular, Inc Due to...
The Issue: Selected lots of the Fill Polymer Kit (European Model Number: TVFP14- B) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling Recalled by...
The Issue: American Medical Systems¿ (AMS) is issuing a voluntary recall on a number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Sliced CT Scanner System Recalled by Philips And Neusoft...
The Issue: The four screws that secure the patient table top to the carrier pulled out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...
The Issue: Complaint received from sales representative that the drill guide tubes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.