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 23441–23460 of 27,456 recalls
Recalled Item: SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory...
The Issue: The interface fails to send abnormal flags for Lab test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw...
The Issue: Small Bone Innovations (SBi) is recalling all lots of 3.0/4.0mm AutoFIX"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerSys¿ Hip System Recalled by Zimmer, Inc. Due to During routine...
The Issue: During routine inspection, beaded hip stem forgings received from supplier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number...
The Issue: Blade can shift during shipping which makes the product ineffective.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accell Evo3C Demineralized Bone Matrix Recalled by Integra LifeSciences...
The Issue: This lot of Accell Evo3C Demineralized Bone Matrix, 5cc was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser...
The Issue: Laser Aperture label was not applied to certain GYC-1000 Green Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Resuscitator Bag Series: AF1000 Recalled by Ventlab LLC Due to The...
The Issue: The pop-off valve in the defective devices remain open and a squeeze of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part...
The Issue: Alcon CUSTOM-PAK which is supposed to contain a 27G Anterior Chamber Cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.