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 2680126820 of 47,970 recalls

DrugAugust 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...

The Issue: Defective Delivery System: Products no longer meet the release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2017· Lucky Mart Inc.

Recalled Item: PIYANPING Anti-Itch (hydrocortisone) Lotion Recalled by Lucky Mart Inc. Due...

The Issue: Incorrect Product Formulation: product contains dexamethasone instead of...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2017· Amerisource Health Services

Recalled Item: Enalapril Maleate Tablets Recalled by Amerisource Health Services Due to...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 29, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 Recalled by...

The Issue: A limited portion of the lot was manufactured with less than the required...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2017· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The device may exhibit...

The Issue: The device may exhibit premature battery depletion.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2017· St Jude Medical Inc.

Recalled Item: Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q Recalled by St Jude...

The Issue: The device may exhibit premature battery depletion.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee System Product Usage: The Persona Partial Knee Recalled...

The Issue: Potential for the Persona Partial Knee Impactor Pad to fracture.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2017· Zimmer Biomet, Inc.

Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...

The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2017· Zimmer Biomet, Inc.

Recalled Item: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for Recalled by Zimmer...

The Issue: The affected products are labeled and etched as F-44 mm liners; however, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2017· Zimmer Biomet, Inc.

Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...

The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2017· Beckman Coulter Inc.

Recalled Item: Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter...

The Issue: Unpaired lots of AU lyophilized chemistry calibrator level 1 and 2 have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis Recalled by...

The Issue: Within a specific number of Artis zee biplane and Artis Q biplane systems, a...

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

Class II — Potential Health HazardOngoing
FoodAugust 24, 2017· Handsome Brook Farm, LLC

Recalled Item: Handsome Brook Farm Soy-Free Organic Pasture-Raised Eggs Recalled by...

The Issue: Potential for mold contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza systems with SW VB20A Recalled by Siemens Medical Solutions USA,...

The Issue: When a prior study is being replaced in the workflow step, in certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2017· Philips Electronics North America Corporation

Recalled Item: IntelliVue Multi Measurement Server Recalled by Philips Electronics North...

The Issue: Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Mild Healthcare Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Choice Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP Deviations;...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Option Systems Antibacterial Foaming Hand Wash Recalled by Inopak Ltd Due to...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Toothette Oral Care Short Term Oral Swab System with Perox-A- Recalled by...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q.Care Oral Cleansing & Suctioning System q8. Contains 1 Covered Recalled by...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund