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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.
Showing 23741–23760 of 27,456 recalls
Recalled Item: Nonabsorbable Surgical Suture Recalled by Teleflex Medical Due to Product...
The Issue: Product does not meet minimum needle attachment strength requirements; thus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixt Suture Bonded Plus Violet Braided Polyglycolic Acid Coated Suture...
The Issue: Product does not meet minimum needle attachment strength requirements; thus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Fixt Suture Braided Polyester Recalled by Teleflex Medical Due to...
The Issue: Product does not meet minimum needle attachment strength requirements; thus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIO Recalled by Teleflex Medical Due to The product did not meet minimum...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dekna-lok Recalled by Teleflex Medical Due to The product did not meet...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software...
The Issue: The System may go into a controlled failed state if a series of parameters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra CUSA Excel Disposable Wrench. Catalog Number C5601. The CUSA...
The Issue: Some 23 kHz Torque Wrenches were incorrectly assembled and contained a 36...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halogen Lamp component in RetCam 3 System - Clarity Medical Systems Recalled...
The Issue: One lot of Halogen lamps have the potential to fail sooner than the expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent (). The ZYM B reagent is Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FB Reagent (). FB reagent is an additional test Recalled by BioMerieux SA...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: A customer reported that after upgrading to software version 3.5.5 from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NIH (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM 6 Monitor in use with a Multi Parameter Module Recalled by Mindray DS...
The Issue: The MPM included a cardiac ST/Arrhythmia analysis feature which is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Recalled by Mevion Medical Systems, Inc. Due to Geometric...
The Issue: Geometric positioning error can occur after a rotational correction has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...
The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....
The Issue: The outer package label contained the incorrect length of the device. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Oxylog 3000 plus ventilators Recalled by Draeger Medical Systems,...
The Issue: The potentiometers (knobs) for setting the ventilation parameters may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.