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. 2,326 recalls have been distributed to Rhode Island in the last 12 months.
Showing 35901–35920 of 47,970 recalls
Recalled Item: Sorin Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Potential colonization of organisms, including Mycobacteria, in Sorin Heater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Block Versions Used by Dental Offices often to as Recalled by 3M Company -...
The Issue: 3M is initiating a Field Correction to remove the crown indication from all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PYROLA Advanced Joint Formula capsules Recalled by GC Natural Nutrition,...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement...
The Issue: Incorrect product label. The type of Sewing Ring was mislabeled as being a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use....
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP-1020 LipoTower with Aspiration Pump. Medical use. Recalled by MicroAire...
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxySure Model 615 disposable replacement cartridges Recalled by Oxysure...
The Issue: Flow rate of the recalled replacement cartridges does not meet the draft FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Classical R & F system. Recalled by GE...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision RXi 23A/32A Analog System Recalled by GE Healthcare...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision RXi Digital system Recalled by GE Healthcare Due to...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A reported incident of a...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and...
The Issue: The SFD/IDD safety mechanism may not engage properly at the lower range of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro...
The Issue: QC results were out of range resulting in false resistant strains.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...
The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXYCODONE HCl C-II Tablets Recalled by The Harvard Drug Group, LLC Due to...
The Issue: Superpotent Drug: Confirmed customer complaint of a single unit dose blister...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEXIUM¿ (esomeprazole magnesium) Recalled by AstraZeneca Pharmaceuticals LP...
The Issue: Presence of Foreign Tablets/Capsules: Confimed customer compliant by a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...
The Issue: There is a potential issue that could result to collision between the C-arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...
The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.