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. 997 recalls have been distributed to Rhode Island in the last 12 months.
Showing 19181–19200 of 47,970 recalls
Recalled Item: Recalled by Quest Medical, Inc. Due to Additive and Arrest Agent Labels on...
The Issue: Additive and Arrest Agent Labels on the MPS Top Cover Replacement Kit, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 700 100 mL Recalled by Boston Scientific Corporation Due to A labeling...
The Issue: A labeling discrepancy incorrectly labeled AMS 700 100mL Conceal Low Profile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...
The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...
The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...
The Issue: Subpotent Drug: Low Out of specification (OOS) assay results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Memantine Hydrochloride Extended-release Capsules Recalled by The Harvard...
The Issue: Failed Dissolution Specifications: High out of specification result observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bimatoprost Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System Recalled by TELEFLEX...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.