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. 1,798 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,798 in last 12 months

Showing 2718127200 of 47,970 recalls

Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Medline Industries Inc

Recalled Item: Sterile Elastic Esmark Bandage Recalled by Medline Industries Inc Due to...

The Issue: Product did not undergo correct sterilization procedures and may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2017· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Product Usage: is a software system designed for treatment...

The Issue: For the proton QA preparation module in RayStation 6 (including SP1 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100i Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 300 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
DrugJuly 17, 2017· BESTHERBS COFFEE LLC

Recalled Item: New Kopi Jantan Tradisional Natural Herbs Coffee Recalled by BESTHERBS...

The Issue: Marketed without an approved NDA/ANDA: presence of undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 17, 2017· NatureBox, Inc.

Recalled Item: NatureBox Sticks 'n Stones Recalled by NatureBox, Inc. Due to Firm received...

The Issue: Firm received notification that a consumer found a peanut in NatureBox...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 14, 2017· Garden Of Light Inc.

Recalled Item: WOODSTOCK ORGANIC MATCHA VANILLA OATS Recalled by Garden Of Light Inc. Due...

The Issue: Potential for Listeria contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: Diltiazem 125 mg in 0.9% Sodium Chloride Recalled by SCA Pharmaceuticals Due...

The Issue: Lack of Assurance of Sterility: Product made with recalled 0.9% sodium...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 Recalled by...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Adenosine in 0.9% Sodium Chloride 30mL Recalled by Cantrell Drug Company Due...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Glycopyrrolate Injection Solution Recalled by Cantrell Drug Company Due to...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium Chloride 250 Recalled...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Succinylcholine Chloride Injection Solution 5 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: NORepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL from Stock...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCl 25 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine 100 mg in 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL 3 mcg/mL + BUPIvacaine 0.1% in 0.9% Sodium Chloride 250 mL Recalled...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: EPINEPHrine HCl 4 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund