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. 2,533 recalls have been distributed to Rhode Island in the last 12 months.
Showing 5741–5760 of 27,456 recalls
Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...
The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilex Fluid Control System-Intended to provide fluid distension of the...
The Issue: The display of inflow volume can reach its limit of 30,000 ml during long...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare software Recalled by RAYSEARCH LABORATORIES AB Due to An issue was...
The Issue: An issue was found in Software RayCare 5A, 5B, 6A, including service packs,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...
The Issue: May have a battery life lasting less than the full 48 hours, requiring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...
The Issue: Sample misidentification could occur under specific conditions and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...
The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to Lipemic interference...
The Issue: Lipemic interference failed to meet the performance specification listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Air/Water Valve is provided/used with the following Endoscopes:...
The Issue: The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX S Recalled by Medicrea International Due to There is a potential for a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX C+ Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX MANTA Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carina Sub-Acute Care Ventilator Recalled by Draeger Medical, Inc. Due to...
The Issue: Presence of polyether polyurethane (PE-PUR) and emission of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.