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. 1,037 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,037 in last 12 months

Showing 14641–14660 of 47,970 recalls

DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 50 Recalled by...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 Recalled by...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Qikmoov LLC

Recalled Item: Vy&Tea (Vietnamese Labeling with a green leaf and a bird Recalled by Qikmoov...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 70 Recalled by...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 100 Recalled by...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 100+ Recalled...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 Recalled by...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Aveeno Protect + sunscreen weightless spray with oat SPF 60 Recalled by...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 13, 2021· Micro Therapeutics Inc,

Recalled Item: Pipeline Flex Embolization Device Recalled by Micro Therapeutics Inc, Due to...

The Issue: Due to potential push wire fractures in the delivery system during use. The...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2021· Micro Therapeutics Inc,

Recalled Item: EV3 Pipeline Flex Embolization Device with Flex Shield Technology Recalled...

The Issue: Due to potential push wire fractures in the delivery system during use. The...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2021· Stanbio Laboratory, LP

Recalled Item: Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in...

The Issue: Deterioration in the stability of the reagents which has resulted in lower...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2021· Stanbio Laboratory, LP

Recalled Item: Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent. Recalled by...

The Issue: Deterioration in the stability of the reagents which has resulted in lower...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2021· Stanbio Laboratory, LP

Recalled Item: Cardinal Health Beta-Hydroxybutyrate . in vitro diagnostic reagent. Recalled...

The Issue: Deterioration in the stability of the reagents which has resulted in lower...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2021· Stanbio Laboratory, LP

Recalled Item: Beta-Hydroxybutyrate Reagent A - Enzyme (unlabeled). in vitro diagnostic...

The Issue: Deterioration in the stability of the reagents which has resulted in lower...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2021· W. L. Gore & Associates Inc.

Recalled Item: Gore Molding & Occlusion Balloon Catheter Recalled by W. L. Gore &...

The Issue: Complaints received concerning Balloon Catheter leakage from the guidewire...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2021· Abbott Laboratories, Inc

Recalled Item: Alinity s System . An automated immunoassay analyzer for Recalled by Abbott...

The Issue: A design defect (hardware and software) allows liquid waste pressure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2021· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: Due to intermittent failures of the power supply in the ultrasound system...

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

Class II — Potential Health HazardOngoing