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. 1,068 recalls have been distributed to Rhode Island in the last 12 months.
Showing 6601–6620 of 27,456 recalls
Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...
The Issue: Issue related to the operation of the arm latch within the column that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....
The Issue: Error in the Introduction section of the user manual that indicates the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Recalled by Maquet Cardiovascular, LLC Due to Some batches...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R1.1 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeLight Fiber Optic Cable: Clear Recalled by Stryker Corporation Due to...
The Issue: Fiber optic cables assembled with not enough epoxy on the proximal end,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CirClamp with 1.3cm Bell & Insert Reprocessed Recalled by MEDLINE...
The Issue: The CirClamp subassembly found in the kit was the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for Recalled...
The Issue: Not programmed in accordance with specification. The programming affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Scrot Zero 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mild Chromic Gut Absorbable Sutures Recalled by Covidien, LP Due to...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Infr Zero 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Portable Electric Ventilator Recalled by Philips...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator Recalled by...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Portable Electric Ventilator Recalled by Philips Respironics,...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIOX RX15 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...
The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.