Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,053 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
1,053 in last 12 months

Showing 14941–14960 of 49,990 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 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: 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 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 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 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 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
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF...

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: 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
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: 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· 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· 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· Stanbio Laboratory, LP

Recalled Item: Synchron CX/DX/LX Beta-Hydroxybutyrate . in vitro diagnostic reagent....

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 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· 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