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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,351 in last 12 months

Showing 2736127380 of 47,970 recalls

Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Latanoprost PF Solution Recalled by ImprimisRx CA, Inc., dba ImprimisRx Due...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Timolol-Latanoprost PF Solution (0.5-0.005)% Recalled by ImprimisRx CA,...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Curcumin Emulsion 10mg/ml Injection Recalled by ImprimisRx CA, Inc., dba...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Syringe Bulb Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing