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. 2,341 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,341 in last 12 months

Showing 3240132420 of 47,970 recalls

DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 4 mcg/mL Fentanyl Citrate and 0.0625% Bupivacaine HCl (Preservative Free)...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 0.125% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride Recalled...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· KVK-Tech, Inc.

Recalled Item: Benzphetamine Hydrochloride Tablets Recalled by KVK-Tech, Inc. Due to...

The Issue: Discoloration: presence of scuffing marks on tablets.

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

Class III — Low RiskOngoing
Refund
FoodMay 5, 2016· Simply Delicious Inc.

Recalled Item: Bobo's Oat Bars Recalled by Simply Delicious Inc. Due to Simply Delicious is...

The Issue: Simply Delicious is recalling Lemon Poppyseed bars because they were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 5, 2016· Teleflex Medical

Recalled Item: Sterile Sheridan/HVT Cuffed Recalled by Teleflex Medical Due to The labeling...

The Issue: The labeling of some units indicates that it contains a size 7mm tracheal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker PowerPRO (XT Recalled by Stryker Medical Division of Stryker...

The Issue: Complaints of smoke coming from the foot end of the cot. This reportedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Recalled...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 4, 2016· NatureBox, Inc.

Recalled Item: Dark Cocoa Nom Noms 4.5oz. (128g) Recalled by NatureBox, Inc. Due to Firm...

The Issue: Firm was notified by third party warehouse that some Peanut Butter Nom Nom...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Brown & Haley Inc.

Recalled Item: Mountain Thins Trail Mix flavor Recalled by Brown & Haley Inc. Due to...

The Issue: Mountain Thins Trail Mix flavor, net wt. 5.3 oz., is recalled because it...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: VersaFx Femoral Fixation System Hex head compression screw 4.7 mm Recalled...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Manufacturing B.V....

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing