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. 2,517 recalls have been distributed to Rhode Island in the last 12 months.
Showing 9781–9800 of 47,970 recalls
Recalled Item: Tri-Staple 2.0 Black Intelligent Reload Recalled by Covidien, LP Due to...
The Issue: Affected lots have the potential for a broken sled vane, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finished Goods Box of 50 Inserts and Scanning Labels for Recalled by Stryker...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator System Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finished Goods Box of 50 Inserts and Scanning Labels for Recalled by Stryker...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to There...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a Recalled...
The Issue: An observed trend of high conductivity dialysate alarms in a hemodialysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Side Cart Recalled by Intuitive Surgical, Inc. Due to Preventative...
The Issue: Preventative maintenance data was used to identify instrument Arms, part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Large component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Medium component of VS Newborn Recalled by SUREPULSE...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Small component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Extra Small component of VS Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Extra Large component of VS Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clobetasol propionate Cream USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug: Low assay result observed during long-term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Snack Day by Lidl Vanilla Flavored Kettle Corn Drizzled with Recalled by...
The Issue: May contain undeclared peanut residue.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Drizzilicious Mini Rice Cake bites Net Wt. 4oz and/or .74oz Recalled by...
The Issue: May contain undeclared peanut residue.
Recommended Action: Do not consume. Return to store for a refund or discard.