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 1481–1500 of 27,456 recalls
Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross Access Solution (VXSK) Recalled by Boston Scientific Corporation...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...
The Issue: As a result of a comprehensive product performance review it was determine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Manifold Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tubing Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Pressure Tubing: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Waste Management Kit: Recalled by Merit Medical Systems, Inc. Due to...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zvu Anorectal Manometry Procedure Kit Recalled by Diversatek Healthcare Due...
The Issue: Anorectal manometry procedure kit outer kit label is mislabeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Recalled by DRG...
The Issue: An incoming complaint reported that the expiration date on the kit box label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. Fluoroscopic X-Ray System. Recalled by PHILIPS MEDICAL...
The Issue: Potential for bolts connecting the gearbox to the mounting flange of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i SETpoint Calibrator Recalled by Siemens Healthcare...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROSKOP Omnia. Model Number: 10094910 Recalled by Siemens Medical Solutions...
The Issue: A resistor in the frequency inverter may strongly overheat potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.