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. 2,447 recalls have been distributed to Rhode Island in the last 12 months.
Showing 17121–17140 of 47,970 recalls
Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...
The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC Application Software c4D as part of the device Catalyst: Recalled by...
The Issue: PC Application Software c4D not changing Site upon synchronization during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss Meditec AG VISUREF150 - Product Usage: Recalled by Carl Zeiss...
The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss Meditec Ag VISULENS 550 - Product Recalled by Carl Zeiss Meditec...
The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...
The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...
The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...
The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Command Brands GelAnti Bac Instant Hand Sanitizer Recalled by ROQUE PLAST,...
The Issue: CGMP Deviation: Potential contamination with undeclared methanol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Day & Night Pack Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) Recalled by...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Subpotent drug: Out of specification for assay at the 15-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine Recalled by...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ear Pain MD Pain Relief Drops For Kids (lidocaine HCl Recalled by Eosera,...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.