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. 2,314 recalls have been distributed to Rhode Island in the last 12 months.
Showing 37801–37820 of 47,970 recalls
Recalled Item: Siemens Healthcare Caps for capillary 100 uL Recalled by Siemens Healthcare...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2...
The Issue: A device malfunction may cause the biopsy needle to fail to reach the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS Oncology Information System Servers Recalled by Siemens...
The Issue: There is a potential safety risk when using LANTIS server software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to A system freeze-up of...
The Issue: A system freeze-up of the Merge Hemo system, that included the PHASEIN End...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius iNtuition Client Viewer. Findings Workflow module Recalled by...
The Issue: Software anomaly related to RECIST1.1 target lesion evaluation criteria in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis Catheters and PICCs: Product identification: MCDLTSL24P (SF X...
The Issue: Drug products contained within the kits may have been rendered ineffective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Sun Pharma Global Fze...
The Issue: Presence of Particulate Matter: lot is not meeting the specification limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam Recalled by Sun Pharma Global Fze Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: 6 month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 2 mg/0.08 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter; Hospira has identified the particulate as a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Chemistry Systems Drug Calibrator I Recalled by Siemens Healthcare...
The Issue: Incorrect calibrator lot values were assigned for ADVIA Chemistry Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HeartWare Controller) Product Usage:...
The Issue: The affected clinical trial Controllers exhibit a higher susceptibility to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brainlab Offset Cup Impactor Universal. Part of the Brainlab Recalled by...
The Issue: The recommended sterilization and drying parameters are not effective to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard 323 pump Recalled by CME America, LLC Due to CME America is...
The Issue: CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the monitor may fail and requires a power circle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streit's Kids Dark CHOCOLATE Coins Recalled by Aron Streit Inc. Due to...
The Issue: State of New York Department of Agriculture and Markets tested revealed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Archer Farms Cumin Recalled by Brinkhoff & Monoson Inc Due to Undeclared Peanut
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dark Chili Powder packaged in the following configurations: (1) a Recalled...
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: garden lites Southwestern Souffle Recalled by classic cooking llc Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.