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. 2,368 recalls have been distributed to Rhode Island in the last 12 months.
Showing 22881–22900 of 27,456 recalls
Recalled Item: Port Access Kit with MicroClave Clear Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cap Change Kit with MicroClave Clear Connector Recalled by ICU Medical, Inc....
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor...
The Issue: The firm became aware of a potential problem that was initiated by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Split Cath III Trays Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST¿CKERT HeaterCooler System 3T Recalled by Sorin Group USA, Inc. Due to On...
The Issue: On August 1, 2014 Sorin Group USA, Inc. informed consignees via letter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...
The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas IT 1000 Product Usage: Intended Use: An electronic Recalled by...
The Issue: Potential that test results would be assigned to the wrong Patient ID if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray V21 Recalled by Mindray DS USA, Inc. dba Mindray North America Due...
The Issue: Mindray DS USA Inc. initiated a voluntary field corrective action for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...
The Issue: Internal review found that five (5) PFJ implant forgings were identified as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RADIANCE v. 2.4X Recalled by Radiometer America Inc Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illumina Worklist Manager (IWM) (software v1.0.15) Recalled by Illumina Inc...
The Issue: A software component of the MiSeqDx instrument, called the Illumina Worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.