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.

47,970 total recalls
2,521 in last 12 months

Showing 71017120 of 47,970 recalls

DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Rugby brand Lubricating Tears Eye Drops (Dextran 70 0.1% Recalled by Kilitch...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Lubricant Eye Drops (Propylene glycol Eye Drops 0.6%) Recalled...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%) Recalled by Kilitch...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: CVS Health brand Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: EQUATE brand Hydration PF Lubricant Eye Drops (Polyethylene glycol 400...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: CVS Health brand Recalled by Kilitch Healthcare India Limited Due to...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%)...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Dry Eye Relief (Carboxymethylcellulose Sodium 1%) Recalled by...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Rugby brand Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by Kilitch...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Lubricant Gel Drops (Polyethylene glycol 400 0.4% Recalled by Kilitch...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Lubricant Gel Drops (Carboxymethylcellulose sodium 1.0%) Recalled by Kilitch...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Recalled by...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by Kilitch Healthcare...

The Issue: Non-Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· KINDER FARMS LLC

Recalled Item: KinderMed INFANTS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2023· KINDER FARMS LLC

Recalled Item: KinderMed KIDS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC Due...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 13, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...

The Issue: There have been transcription errors on the Instructions For Use (IFU) of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Blue Belt Technologies, Inc

Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...

The Issue: Possibility that the user is unable to resolve drill disconnection error...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Steris Corporation

Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...

The Issue: Identification label on affected hookups could become illegible over time...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Maquet Medical Systems USA

Recalled Item: Venous probe connection cable ( and 701048804) used with Recalled by Maquet...

The Issue: Firm received complaints of breaks in the insulation, shielding, or wires of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing