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. 2,521 recalls have been distributed to Rhode Island in the last 12 months.
Showing 8781–8800 of 27,456 recalls
Recalled Item: Beaver Xstar Crescent Knife Recalled by Beaver Visitec International, Inc....
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle Recalled by Cook Inc. Due to Transseptal needles may...
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wagner: CustomEyes...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ComposiTCP 30 Interference screw D 7- L:25 mm Recalled by SCIENCE & BIO...
The Issue: Mislabeled product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Electrodes Recalled by 3M Company - Health Care Business Due to...
The Issue: Potential for breakage of the ECG electrode carbon stud from the eyelet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis/ Sensis Vibe systems with software VD1X as follows: (1)Sensis...
The Issue: System operator manual states that the system should be rebooted once, every...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE...
The Issue: Due to component (housing and plunger) detaching from the semi-automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cliquid MD version 3.4 software used in conjunction with Analyst Recalled by...
The Issue: The values of the Internal Standard (IS) concentrations are incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellume COVID-19 Home Test Recalled by ELLUME LTD Due to Due to a higher rate...
The Issue: Due to a higher rate of false positive test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.020 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.010 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR Saline-Filled Breast Implants are constructed from room temperature...
The Issue: Due to a manufacturing issue, Implant may have a potentially weakened area...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT i1000SR /1L86 and 1L87 Recalled by Abbott Laboratories Due to...
The Issue: Twelve software-related issues affecting software version 9.41 and earlier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 /2P24 Recalled by Abbott Laboratories Due to Twelve...
The Issue: Twelve software-related issues affecting software version 9.41 and earlier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.