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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.
Showing 25421–25440 of 47,970 recalls
Recalled Item: Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW Recalled by...
The Issue: Slot screw had an overall length of 15mm, but per the specification, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 015 Recalled by Straumann Manufacturing, Inc. Due to A...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E80 ultrasound system Vivid E80 / E90 / Recalled by GE Medical...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid 7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E95 ultrasound system Product The device is intended Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ 9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ E9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E90 ultrasound system Product Usage: Vivid E80 / Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Lithium Heparin Green Top Tube Recalled by Becton Dickinson &...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ EDTA Pink Top Tube Recalled by Becton Dickinson & Company Due...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 Recalled...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ EDTA Tan Top Tube Recalled by Becton Dickinson & Company Due...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ MULTI 1 SDIL Recalled by Siemens Healthcare Diagnostics,...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ MULTI 2 SDIL Recalled by Siemens Healthcare Diagnostics,...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ CTNI Sample Diluent Recalled by Siemens Healthcare...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Pepper Est. 1885 Diet Recalled by Swire Coca Cola USA Due to Foreign...
The Issue: Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GFS Belgian Mini Chocolate Topped Eclairs Recalled by Poppies International...
The Issue: Products may be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fabior (tazarotene) Foam Recalled by Mayne Pharma Inc Due to Superpotent...
The Issue: Superpotent Drug: High out of specification results for tazarotene assay at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.