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 8181–8200 of 27,456 recalls
Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Microbiology Informatics Solution Recalled by Becton Dickinson &...
The Issue: When updating BD Kiestra customers to BD Synapsys version 4.10, the custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RocheDiabetes Care Platform Software version 2.5.2 material number...
The Issue: Potential for patient data mismatch when using browser "back" button to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 10mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 12mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Standard PVC Laryngeal Masks Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The mask cuff may disconnect from the device's breathing tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-MP60: OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-3C160: EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-MP160F: EVIS EXERA Bronchofibervideoscope Recalled by Olympus Corporation...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-1TQ180: EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product Recalled by SIMPLIVIA...
The Issue: Disconnection of the OnGuard2 Bag Adaptor SP from infusion bags which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT STAT Myoglobin Calibrators Recalled by Abbott Laboratories Due to...
The Issue: This calibrator lot did not meet acceptance criteria during ongoing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acuson 9vE4 Transducer Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: Transducers (component of ultrasound system) may exceed recommended thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now...
The Issue: Software error may result in sporadic problems causing scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.