Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,623 recalls have been distributed to Arkansas in the last 12 months.
Showing 9201–9220 of 28,355 recalls
Recalled Item: AMSORB PLUS PREFILLED G-CAN 1.0L Recalled by Armstrong Medical Services...
The Issue: Some devices may be associated with high and unexpected resistance to gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...
The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...
The Issue: Customers have reported an increased number of false positive SARS-CoV-2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...
The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...
The Issue: There is potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...
The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uEXPLORER PET/CT System - Product Usage: intended to be operated Recalled by...
The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow sensors that may be installed in the following GEHC Recalled by GE...
The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uMI 550 System - Product Usage: intended to be operated Recalled by Shanghai...
The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow sensors kept as stand-alone user replaceable spare parts for Recalled...
The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite Recalled by CAREFUSION Due...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented Recalled by...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Recalled by...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES Recalled by...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SmartSite Bag Access Device Recalled by CAREFUSION Due to Needle-free...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.