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. 1,017 recalls have been distributed to Rhode Island in the last 12 months.
Showing 17121–17140 of 47,970 recalls
Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ Recalled by Open...
The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC...
The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) Recalled...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 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: 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: 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: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...
The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System. The EtCO2 module is a capnograph indicated for continuous...
The Issue: Infusion pump component defect may result in interruption of patient monitoring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your 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.