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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.
Showing 25601–25620 of 27,456 recalls
Recalled Item: Bracket Buccal Tube U7L DB/UL22 Roth MT HK 0/-14/0 Product Recalled by...
The Issue: Ormco Corporation is voluntarily recalling one (1) lot of Bracket Buccal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDICYCL-E- Lite Portable Oxygen System An integrated portable oxygen...
The Issue: A number of MEDICYL-e Portable Oxygen Systems may have misapplied valve flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture Recalled by...
The Issue: A post market safety review following several customer complaints indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Systems with Software Artis VC20x/VC21A/VD10x that have a DSA Recalled...
The Issue: The firm has become aware of a potential issue on Artis systems with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.5 MM LCP(R) Distal Humerus System The Synthes 3.5 Recalled by...
The Issue: Recall is being initiated due to the part being mislabeled (Part Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare Pump Model 4200 PCA Infuser makes possible the Recalled by...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA 3 Recalled by Hospira Inc. Due to Screw rotation error...
The Issue: Screw rotation error occurring when the pump detects a mismatch between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA Infusion System with Hospira MedNet Software Recalled by...
The Issue: Screw rotation error occurring when the pump detects a mismatch between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA infusion system with Hospira MedNet software allows clinicians...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PCA 3 system cam be used in a wide range of clinical settings Recalled...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA Plus II infusion pump system is designed for safe Recalled...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent" irrigation tubing. Product Usage: The Torrent irrigation system...
The Issue: The firm was notified by their customers that there was a water leakage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version...
The Issue: It has come to the attention of MAQUET that there have been episodes of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge Group battery modules for use with Maquet SERVO-i Recalled by...
The Issue: When using the SERVO-i on battery power, in a very small number of cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1...
The Issue: Customer complaint investigation confirmed the issue of false skipped wells...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a...
The Issue: Unapproved medical device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has identified potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has received reports of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....
The Issue: The recall was initiated because Alere San Diego has an update for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner....
The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.