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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.
Showing 2001–2020 of 27,456 recalls
Recalled Item: Baxter TruSystem 7500 Hybrid (SC) Recalled by Baxter Healthcare Corporation...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Stationary column TruSystem 7500 U Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid MR IMRIS Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Operating table column TS7500 MOBIUS Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed Surfaces Recalled by Baxter Healthcare Corporation Due to The...
The Issue: The air bladders inside the mattress may move out of position when the head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid (FC) Recalled by Baxter Healthcare Corporation...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid Plus (SC) Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Floor mounting column TruSystem 7500 Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Floor mounting column TS 7500 U Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...
The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.