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. 2,457 recalls have been distributed to Rhode Island in the last 12 months.
Showing 15101–15120 of 27,456 recalls
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...
The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...
The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...
The Issue: Incorrect expiration being entered for one lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...
The Issue: The analyzer software may cause a mis-match of patient demographics and test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...
The Issue: Charging base may overheat with localized melting and sparking, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...
The Issue: The device and its accessories may not have been manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...
The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Infinity XR2 Base Unit-Extended Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: In rare cases of insufficient maintenance or high clinical workload, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system Recalled by...
The Issue: If the beam model has a highly asymmetric primary source, it is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pure Rayz Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not receive...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Quasar Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.