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. 1,673 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,673 in last 12 months

Showing 4276142780 of 47,970 recalls

Medical DeviceSeptember 10, 2013· Aesculap, Inc.

Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...

The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Beckman Coulter Inc.

Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...

The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Beckman Coulter Inc.

Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...

The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Becton Dickinson & Co.

Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...

The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...

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

Class II — Potential Health HazardOngoing
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Vancomycin PF (BSS) 1% Recalled by Avella of Deer Valley, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund