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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,351 in last 12 months

Showing 2292122940 of 27,456 recalls

Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 D8L OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Becton Dickinson & Company

Recalled Item: BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection Recalled...

The Issue: BD received some reports of open seals found on the BD Posiflush SF Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Abbott Laboratories

Recalled Item: ICT Serum Calibrator . For use in the calibration Recalled by Abbott...

The Issue: ICT Serum Calibrator may generate lower than expected Potassium Quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...

The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· GF Health Products, Inc./d.b.a.Basic American Metal Products

Recalled Item: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...

The Issue: The bed head deck may fail to elevate as expected during normal operation....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Diagnostica Stago, Inc.

Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....

The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Zimmer, Inc.

Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension EXL Integrated Chemistry System in vitro diagnostic...

The Issue: The Reagent Lid hinge may lose its effectiveness and slowly shift downward...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· Market-Tiers Inc

Recalled Item: Instructions for Use for the blue endo MOREsolution Electromechanical...

The Issue: Some pages of the Instructions for Use were omitted, including pages...

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

Class II — Potential Health HazardOngoing