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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.
Showing 1761–1780 of 27,456 recalls
Recalled Item: iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Recalled by Medical...
The Issue: Potential for DC Power Supply housing to become hot to the touch and deform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Occlusion Catheter. Catalog Numbers: 2103-36 Recalled by LeMaitre...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X)...
The Issue: Potential for the presence of visible foreign matter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09 Recalled by...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Craniotomy Kit Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator Recalled by Integra LifeSciences Corp....
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355 Recalled...
The Issue: Field action to clarify the flow rates and inlet fluid temperatures, along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...
The Issue: Adapters may disconnect during setup or while in use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMS8000 Patient Monitor Recalled by Contec Medical Systems Co., Ltd. Due to...
The Issue: Patient monitor has nine identified cybersecurity vulnerabilities.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...
The Issue: Adapters may disconnect during setup or while in use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis HPCA Ambulatory Infusion Pump Recalled by Smiths Medical ASD,...
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis VIP Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT Recalled by...
The Issue: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis Infusion Pump Models: 1) PUMP KIT Recalled by Smiths Medical ASD,...
The Issue: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Solis HSPCA Pump Recalled by Smiths Medical ASD, Inc. Due to Pumps may...
The Issue: Pumps may experience Wireless Connection Modules intermittent connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blueprint Software Recalled by Tornier S.A.S. Due to A software bug in...
The Issue: A software bug in Blueprint version 4.2.1 prevents users from accessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile Weitlaner Retractor 3 x 4 Prong Recalled by MEDLINE...
The Issue: Three is the potential for the retractors to puncture through the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: Four (4) total reports were sent to customers with clinically relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile Weitlaner Retractor Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Three is the potential for the retractors to puncture through the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.