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. 1,970 recalls have been distributed to Rhode Island in the last 12 months.
Showing 7461–7480 of 47,970 recalls
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO EMPOWR Knee Punch Handle Recalled by Encore Medical, LP Due to Knee...
The Issue: Knee punch handle tip is breaking during surgery due to the lack of heat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ION*Sinus Spray Recalled by Biomic Sciences, LLC dba ION Intelligence of...
The Issue: Microbial contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ION* Sinus Support Nasal Spray Recalled by Biomic Sciences, LLC dba ION...
The Issue: Microbial contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Restore Sinus Spray Recalled by Biomic Sciences, LLC dba ION Intelligence of...
The Issue: Microbial contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Injectable Suspension Recalled by Eugia US LLC Due...
The Issue: Presence of Particulate Matter: A product complaint of a piece of glass was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gynazole-1 Recalled by Padagis US LLC Due to Incorrect Product Formulation:...
The Issue: Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP Recalled by Olympus Corporation...
The Issue: Fiberscopes do not have adequate data to support that the suction flow rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS CONSTRAINED ARTICULAR INSERT Size 5-6 Recalled by Smith &...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Recalled...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope Recalled by Boston Scientific...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS ARTICULAR INSERT Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The...
The Issue: Due to a software anomaly which potentially could result in the surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SA3000 VENTED MICRO SPIKE ADAPTER Recalled by B. Braun Medical, Inc. Due to...
The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.