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. 2,262 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,262 in last 12 months

Showing 4790147920 of 47,970 recalls

FoodApril 7, 2009· Trophy Nut Co Inc

Recalled Item: Trophy Nut Brand 1.5 oz. tube Recalled by Trophy Nut Co Inc Due to Potential...

The Issue: The product is being recalled because it was manufactured using pistachios...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 7, 2009· Trophy Nut Co Inc

Recalled Item: Trophy Nut Brand 6 oz. natural pistachios Recalled by Trophy Nut Co Inc Due...

The Issue: The product is being recalled because it was manufactured using pistachios...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 7, 2009· Trophy Nut Co Inc

Recalled Item: Wa Wa brand 6 oz. Pistachio Gusset Recalled by Trophy Nut Co Inc Due to...

The Issue: The product is being recalled because it was manufactured using pistachios...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 6, 2009· Stellate Systems

Recalled Item: Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Recalled by...

The Issue: The firm is initiating this recall because the implied or stated indications...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2009· Invatec Llc

Recalled Item: lnvatec SpA brand Diver C.E. Recalled by Invatec Llc Due to Devices labeled...

The Issue: Devices labeled for an intended use was not included in the existing 510(k)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2009· Zynex Medical, Inc.

Recalled Item: IF 8000 Recalled by Zynex Medical, Inc. Due to Zynex notified customers that...

The Issue: Zynex notified customers that a malfunction in the IF 8000 can result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 4.5mm x 35mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: Screw Tulip Recalled by NuVasive Inc Due to The tulip portion of the screw...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing