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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.
Showing 24581–24600 of 47,970 recalls
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Failed...
The Issue: Failed Stability Specifications: lot out of specification for elevated water...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent Drug and Failed Stability Specifications: lot out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent Drug: lots out of specification for elevated sodium chloride and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...
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: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P400 PREM U/M 18FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEMP SENSE SILICONE 14FR5CC2W Recalled by COVIDIEN LLC Due to The...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P400 PREM U/M 16FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...
The Issue: The temperature sensor catheters may be defective in that they will show a...
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: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...
The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A nonsterile bulk product designated for further processing in a tray was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.