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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.
Showing 24601–24620 of 27,456 recalls
Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model#...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ Flex Femoral Component. Provides increased flexion capability....
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...
The Issue: Imprecision with certain lots
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sidus" Head (Not distributed in the United States) Recalled by Zimmer, Inc....
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vented Spike Adapter Product Code 2C0471 Recalled by Baxter Healthcare Corp....
The Issue: Potential tears in the pouch of six lots of Vented Spike Adapter Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...
The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code:...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...
The Issue: It was discovered that Carestream received a report from a customer that 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...
The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.