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. 929 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
929 in last 12 months

Showing 42921–42940 of 47,970 recalls

DrugAugust 29, 2013· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (TM) IBUPROFEN Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or missing lot and/or exp date- This product is being...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Hospira Inc.

Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter; report of visible particulates in the glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Cubist Pharmaceuticals, Inc.

Recalled Item: Cubicin (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter; Glass particulates observed in vials

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 29, 2013· Blythedale Farm Inc.

Recalled Item: Blythedale Farm Vermont Brie Recalled by Blythedale Farm Inc. Due to...

The Issue: Inadequate pasteurization

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 29, 2013· Blythedale Farm Inc.

Recalled Item: Blythedale Farm Farmstead Brie Recalled by Blythedale Farm Inc. Due to...

The Issue: Inadequate pasteurization

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 29, 2013· Blythedale Farm Inc.

Recalled Item: Blythedale Farm Camembert Vermont Recalled by Blythedale Farm Inc. Due to...

The Issue: Inadequate pasteurization

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 28, 2013· Zimmer, Inc.

Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...

The Issue: Based on a review of historic packaging validations, it was determined that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Globus Medical, Inc.

Recalled Item: Globus Medical MicroFuse Putty Recalled by Globus Medical, Inc. Due to The...

The Issue: The sterility of this product to a Sterility Assurance Level (SAL) of 10(-6)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Extension Shims Extension shims are manufactured from grade 5...

The Issue: Fit variation among all lots of S-LIFT extension shims with corresponding...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Carefusion 2200 Inc

Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...

The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· 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 potential safety issue...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...

The Issue: When using systems operating with software versions VD10A/G during a RAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· H & H Associates

Recalled Item: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H &...

The Issue: Medical device tubing used for endotracheal airway application may become...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 27, 2013· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Captia Syphilis-G Test Kit Product Usage: This is an enzyme Recalled by...

The Issue: Trinity Biotech recalled Trinity Biotech Captia Syphilis IgG kits due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Zimmer, Inc.

Recalled Item: Zimmer Title 2 Bone Screw Remover Instrument Recalled by Zimmer, Inc. Due to...

The Issue: Possibility of the weld to the quick-connect breaking when force is applied...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Snug Seat Inc

Recalled Item: Crocodile (size 3) are two-armed Recalled by Snug Seat Inc Due to The bolts,...

The Issue: The bolts, which secure the handles, on the Crocodile (size 3) could break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

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

Class II — Potential Health HazardOngoing