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. 2,341 recalls have been distributed to Rhode Island in the last 12 months.
Showing 33101–33120 of 47,970 recalls
Recalled Item: Ossur Lil Angel Vest P3 Lambswool. Pediatric sized vest is Recalled by Ossur...
The Issue: There is a potential for partial or complete fracture of the plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV Catheter Kit under the following labels: 1) 3F...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Lil Angel Vest P2 Sorbatex. Pediatric sized vest is Recalled by Ossur...
The Issue: There is a potential for partial or complete fracture of the plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...
The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 Recalled by...
The Issue: Integra's post QA release review of historical product release test results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After importing segmentation results of the left atrium created on the Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...
The Issue: The units have been fitted with a potentially faulty power supply cable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient Recalled...
The Issue: CGMP Deviations: active pharmaceutical ingredient intermediates failed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SODIUM IODIDE I 131 CAPSULE Recalled by Jubilant Draximage Inc Due to...
The Issue: Labeling: Label Error on Declared Strength
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HIgH-Flo Subcutaneous Safety Needle Sets Recalled by Repro-Med Systems, Inc....
The Issue: On 2/24/2016 during post sterilization inspection of part number F180...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom60 Precision Flow Rate Tubing Sets Recalled by Repro-Med Systems,...
The Issue: On 2/24/2016 during post sterilization inspection of part number F180...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to If the PDM is...
The Issue: If the PDM is utilized to output a pressure for computing fractional flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008 Series Hemodialysis Delivery Systems: 2008T Recalled by...
The Issue: Added Warning Statement: Fresenius 2008 Series Hemodialysis Machines False...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiGiorno pizzeria thin crust spinach & mushroom pizza Recalled by Nestle USA...
The Issue: Nestle is recalling a limited number of DiGiorno, Lean Cuisine, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stouffer's vegetable lasagna. Keep Frozen. Sold in the following sizes...
The Issue: Nestle is recalling a limited number of DiGiorno, Lean Cuisine, and...
Recommended Action: Do not consume. Return to store for a refund or discard.