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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.
Showing 901–920 of 27,456 recalls
Recalled Item: InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure Recalled...
The Issue: InSure ONE failed sensitivity testing when used with Test Card Lot T241102,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Software Builds 3.1.3 Recalled by ELEKTA...
The Issue: When appending a care plan that contains one or more wave medication orders,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent Recalled by Beckman...
The Issue: Beckman Coulter has identified that there is an increased probability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oral Probe (Product code 02893-000) Recalled by Baxter Healthcare...
The Issue: Affected oral/axillary probes were inadvertently programmed with the rectal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400...
The Issue: Instructions for use for a foot plating system is being updated to remove...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phasitron 5 Recalled by Percussionaire Corporation Due to IFU update;...
The Issue: IFU update; in-line valve, with pressure relief seal may leak when used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalyft PL & PL40 Expandable Interbody System labeled as follows Recalled...
The Issue: Expandable interbody system cage may loose height or collapse (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number:...
The Issue: Due to two distinct issues: 1. During patient admission, patient demographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Planner Recalled by Surgical Theater Inc Due to A software anomaly,...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuRgical Planner (SRP) Recalled by Surgical Theater Inc Due to A software...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP)...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Navigation Advanced Platform (SNAP) Recalled by Surgical Theater...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Navigation Advanced Platform Patient Engagement (PE SNAP) Recalled...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) labeled as the following with...
The Issue: Potential for Automated Impella Controller (AIC) purge pressure issues due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...
The Issue: Due to complaints of increased resistance when advancing the dilator within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.