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. 2,489 recalls have been distributed to Rhode Island in the last 12 months.
Showing 12841–12860 of 27,456 recalls
Recalled Item: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 -...
The Issue: Due to low Quality Control recovery and invalid Calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Recalled...
The Issue: Due to low Quality Control recovery and invalid Calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and...
The Issue: The firm received a report of an atypical dataset being generated. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...
The Issue: The instrument holder may be sent on a trajectory that is not within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...
The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...
The Issue: The recall is being conducted due to a potential defective component on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...
The Issue: The touchpad may not work properly after cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Express Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Insight Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...
The Issue: The firm received reports of loss of audio alarm after a power failure or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPROTTE Lumbar with Introducer Recalled by Pajunk GmbH Due to Problem with...
The Issue: Problem with packaging sealing process which affects sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.