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. 1,762 recalls have been distributed to Rhode Island in the last 12 months.
Showing 31861–31880 of 47,970 recalls
Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T095-022 Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker AutoPlex System. Model Numbers 0607-687-000 Recalled by Stryker...
The Issue: The Piston Head can become separated from the Delivery Piston, blocking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T105-000WC IV Set w/2 Y-Sites Recalled by WalkMed Infusion, LLC Due to...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...
The Issue: The pouch label was missing the use by date (UBD) of 2018-04.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...
The Issue: Not Ready To Eat IQF Peas and Carrots are recalled because they have a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...
The Issue: Not Ready To Eat IQF Mixed Vegetables are recalled because they have a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...
The Issue: Not Ready To Eat IQF green peas are recalled because they have a potential...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...
The Issue: Not Ready To Eat IQF Sysco Classic Peas & Onions are recalled because they...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Methylprednisolone Tablets Recalled by Jubilant Cadista Pharmaceuticals,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxacillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Presence of Particulate Matter; The firm received two product complaints for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SECONAL SODIUM (secobarbital sodium) Capsules Recalled by Valeant...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dako HER2 CISH pharmDx Kit Recalled by Dako North America Inc. Due to An...
The Issue: An incorrect HER2 probe concentration was used when producing the probe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TSP Hip Fracture Plating System device Recalled by Biomet, Inc. Due to...
The Issue: The screw may fracture at the junction of the shaft and the head during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...
The Issue: There is a potential for stylet stiffening that is not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preamendments device-Sarns Dual Cooler-Heater. The Sarns Dual Cooler-Heater...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System Controller Product Usage: For use as...
The Issue: Loose connector ports in controller body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.