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. 2,515 recalls have been distributed to Rhode Island in the last 12 months.
Showing 10701–10720 of 27,456 recalls
Recalled Item: Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic...
The Issue: Specific lots of MEDRAD Stellant FLEX 150 mL syringe kits may have holes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elastic Traction Device Recalled by Micro-Tech Usa Due to FDA has informed...
The Issue: FDA has informed Micro-Tech that the Elastic Traction Device is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with S. epidermidis E. coli and S. warneri.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Recalled by...
The Issue: Potential contamination with Escherichia coli Staphylococcus epidermidis and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO DISK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with Escherichia coli, Staphylococcus epidermidis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...
The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COAPTITE Injectable Implant Recalled by Merz North America, Inc. Due to The...
The Issue: The Instructions for Use (IFU) updated 03/02/2020 does not match data listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Monitoring Unit (BMU 40) Recalled by Maquet Cardiovascular Us Sales,...
The Issue: The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...
The Issue: Due to a change in handle material and process, probe handle may crack.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 230 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osteosynthesis Compression Staple EasyClip Recalled by Stryker GmbH Due to...
The Issue: The device has the potential to release nickel above the acceptable margin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien MONOJECT Standard Hypodermic Needle Recalled by Cardinal Health...
The Issue: Potential for the needle to detach from the cartridge after the bottom of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...
The Issue: The device may be incorrectly laser marked as a right stem, when it should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...
The Issue: The device may be incorrectly laser marked as a right stem, when it should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.