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. 2,262 recalls have been distributed to Rhode Island in the last 12 months.
Showing 46401–46420 of 47,970 recalls
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX Distributed by ETHICON ETHICON Recalled...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam 4.1. Radiation treatment planning software designed...
The Issue: During the planning process the beam weights can be changed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett Mira. Mobile X-Ray System. Recalled by Siemens Medical...
The Issue: During regular product monitoring, Siemens has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...
The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Armada 35/ Armada 35 LL PTA Catheters. The device is Recalled by Abbott...
The Issue: Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protein Shots Recalled by Protica, Inc Due to Product not sufficiently...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protein Wave 15 grams of protein Recalled by Protica, Inc Due to Product not...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vital Signs Disposable General Purpose 9 French Temperature Probe For...
The Issue: There is a potential for epistaxis during use of the Disposable General...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm...
The Issue: The firm recalled the device after learning of a possible deviation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Recalled by J & J Snack...
The Issue: Luigi's Real Italian Ice Birthday Cake Flavor is mislabeled as "Dairy-Free".
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...
The Issue: The recall was initiated because Karl Storz has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...
The Issue: Shipped with incorrect software
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROmorphone HCl Injection Recalled by Hospira Inc. Due to Superpotent...
The Issue: Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.