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 4666146680 of 47,970 recalls

Medical DeviceJuly 13, 2012· Baxter Healthcare Corp.

Recalled Item: AUTOMIX 3+3 Compounder System Recalled by Baxter Healthcare Corp. Due to...

The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2012· Intuitive Surgical, Inc.

Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...

The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Intuitive Surgical, Inc.

Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...

The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Intuitive Surgical, Inc.

Recalled Item: ACCESSORY BASE STARTER KIT Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Intuitive Surgical, Inc.

Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...

The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Intuitive Surgical, Inc.

Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...

The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Intuitive Surgical, Inc.

Recalled Item: INSTRUMENT ARM DRAPE IS2000 Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Hospira Inc.

Recalled Item: Hospira LifeShield Latex-Free 100 mL Burette Set Recalled by Hospira Inc....

The Issue: The float valve in the burette sticks to the burette wall and does not open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Westone Laboratories, Inc.

Recalled Item: Oto Ease by Westone Recalled by Westone Laboratories, Inc. Due to Westone is...

The Issue: Westone is recalling all Oto Ease ear lubricant in all packaging...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Organic Mild Salsa Recalled by Pulmuone Wildwood Inc Due to The...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Organic Medium Salsa Recalled by Pulmuone Wildwood Inc Due to The...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Hot Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa - Canada (containing...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a number of potential issues...

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

Class II — Potential Health HazardOngoing