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. 2,457 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,457 in last 12 months

Showing 1440114420 of 27,456 recalls

Medical DeviceOctober 31, 2018· COVIDIEN LLC

Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...

The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2018· Horiba Instruments Incorporated

Recalled Item: Clinical Chemistry Recalled by Horiba Instruments Incorporated Due to...

The Issue: Potential for chemical analyzer to report abnormal results due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: This recall has been initiated due to a possible leakage of a hose in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2018· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...

The Issue: There is a potential for blood leakage at the blood inlet connector when...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2018· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...

The Issue: There is a potential for blood leakage at the blood inlet connector when...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...

The Issue: Potential metal burrs in the holes of the device preventing the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Pressure Sentinel¿ Intramedullary Reaming System Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Pressure Sentinel¿ Intramedullary Reaming System Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice...

The Issue: Software defect: For Helical scan with ClearView function, when small arc...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing