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. 2,489 recalls have been distributed to Rhode Island in the last 12 months.
Showing 12261–12280 of 27,456 recalls
Recalled Item: Prometra II Programmable 20mL Pump. Catalog No. 93827 The device Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II 40mL Pump. Catalog No. 16827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225...
The Issue: The manufacturer identified a risk that their products might fail to comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wave Prep Tubes (1710-03) and single use cups (17--00-24) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...
The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...
The Issue: Potential for the expiration date on the outer label that was applied by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Firm has received customer complaints regarding failed calibrations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1 Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Set- PR-35052-HPHNM Recalled by Arrow International Inc Due to Product...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1 Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Central Venous Catheterization Kit ASK-04200-UPM Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT JH-05500 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.