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. 2,269 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,269 in last 12 months

Showing 4434144360 of 47,970 recalls

Medical DeviceMay 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CRP Slides (Reagent) Recalled by Ortho-Clinical...

The Issue: While performing interval testing Ortho Clinical Diagnostics (OCD)...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products K+ (Potassium) Slides (Reagent) Recalled by...

The Issue: While performing interval testing, Ortho Clinical Diagnostics (OCD)...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2013· ConBio, a CynoSure Company

Recalled Item: Multilite Dye Handpieces Recalled by ConBio, a CynoSure Company Due to An...

The Issue: An inconsistency was identified related to electronic display identification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope (GVL) 3 Recalled by Verathon, Inc. Due to...

The Issue: Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8 mm Monopolar Curved Scissors (a.k.a. Hot Shears) Manufactured and Recalled...

The Issue: Intuitive Surgical has identified a potential for some units of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Maryland Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Precise Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Fenestrated Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· DePuy Orthopaedics, Inc.

Recalled Item: DePuy LifeLiner Stick & Cut Resistant Gloves Rt Recalled by DePuy...

The Issue: LifeLiner Stick and Cut Resistant Gloves are being recalled because cases...

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

Class III — Low RiskOngoing
DrugMay 7, 2013· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL) Recalled...

The Issue: Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Supplement Plus Calcium Recalled by Novartis Consumer Health...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Plus Heart Health Non-Thickening Powder Recalled by Novartis...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Supplement Recalled by Novartis Consumer Health Due to The...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Non-Thickening Powder Recalled by Novartis Consumer Health Due to...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 7, 2013· SpineFrontier, Inc.

Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...

The Issue: Potential for set screw to be come deformed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing