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. 2,390 recalls have been distributed to Rhode Island in the last 12 months.
Showing 18881–18900 of 27,456 recalls
Recalled Item: Neural Signal Amplifier. Part Numbers: 4208 Recalled by Blackrock...
The Issue: Blackrock Microsystems, LLC announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triple Line SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir and 2 Recalled...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir Recalled by...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bifurcated SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Reservoir and 2 Blood Sampling...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Monitoring Kit with 30mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TP4 Kit with 10cc SafeSet Reservoir Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Kit with SafeSet and 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Trifurcated Monitoring Kit with 84" SafeSet Reservoir Recalled...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Monitoring Kit with SafeSet 84" Arterial Pressure Tubing...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Monitoring Kit with 03 ml Squeeze Flush Recalled by ICU Medical,...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Bifurcated Kit with SafeSet Reservoir Recalled by ICU Medical,...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Soft Tissue Sleeve Guide Recalled by Zimmer Biomet, Inc. Due...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Targeting Arm Guide Recalled by Zimmer Biomet, Inc. Due to Old...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...
The Issue: Communication provided to emphasize that the PSA values should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Recalled by...
The Issue: Contents of the package do not match the product labeling. Product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 Recalled by Mentor...
The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.