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. 2,314 recalls have been distributed to Rhode Island in the last 12 months.
Showing 39761–39780 of 47,970 recalls
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.
Recalled Item: Carob Supergreens Chunks of Energy (10# ) Recalled by Dancing Star LLC Due...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Date Flax with Turmeric Chunks of Energy (10# ) Recalled by Dancing Star LLC...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk organic Carob powder (10# ) Recalled by Dancing Star LLC Due to...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
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.
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.
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.
Recalled Item: All sterile products within expiry Recalled by Unique Pharmaceutical, Ltd...
The Issue: Lack of Sterility Assurance: A recent FDA inspection revealed poor aseptic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: N-Acetyl Cysteine 20% 4 mL Vial Stock Code: 4133 Recalled by Unique...
The Issue: Non-Sterility: One lot of N-Acetyl Cysteine vials tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
Recalled Item: Clonidine HCl Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Label Error On Declared Strength: The side label description...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.